92 Patient Recruitment Jobs in Hyderabad

As the Associate Director, Pipeline Operations at Novartis, your role is crucial in driving operational excellence and innovation across the Development department. You will lead the delivery of high-quality project and pipeline data, translating insights into actionable outcomes for stakeholders. Your responsibilities include managing and optimizing the Horizon platform and related systems to empower teams in executing drug development projects with precision and agility. Additionally, you will champion the adoption of best practices in project management and collaborate with Biomedical Research (BR) to unlock synergies. Key Responsibilities: - Maintain and optimize the PPM platform and related project management systems to ensure robust operational capabilities for Development. - Act as the primary contact for the PPM/Horizon user community, offering expert guidance on Development Plans setup and management to meet governance and project management requirements. - Establish and enhance centralized project management processes, ensuring alignment with organizational standards and best practices. - Design and implement quality checks to ensure adherence to approved procedures and support data integrity in project plans and processes. - Collaborate with line functions and cross-divisional teams to drive initiatives that enhance data quality, process consistency, and operational efficiency. - Gather and address user feedback to enhance PPM/Horizon usability and contribute to the Horizon training strategy to promote best practices and cross-functional planning. - Support portfolio governance by recording IMB/Board decisions in Horizon and ensuring consistent execution of governance processes. - Contribute to project and portfolio reporting strategies, aiding in the development and implementation of PPM reports for senior management and Development Leadership Team reporting needs. Qualifications Required: - A graduate life science degree (masters or equivalent); Data science understanding is advantageous. - Minimum of 8-10 years of industry experience, with at least 5 years in multi- or cross-functional team roles, preferably in drug development or related fields. - Strong analytical and critical thinking skills with the ability to influence stakeholders at all levels. - Technical proficiency in PowerPoint and Excel, experience with project management systems, and enthusiasm for leveraging new technologies. - Excellent organizational, time management, interpersonal, and communication skills. - Enthusiasm for learning, adaptability, and a growth mindset. Novartis is committed to diversity and inclusion, creating an inclusive work environment and diverse teams that reflect the patients and communities served. If you require accommodation due to a medical condition or disability during the recruitment process, please reach out to diversityandincl.india@novartis.com with your request and contact information. Join the Novartis network to explore suitable career opportunities and benefits that support personal and professional growth. As the Associate Director, Pipeline Operations at Novartis, your role is crucial in driving operational excellence and innovation across the Development department. You will lead the delivery of high-quality project and pipeline data, translating insights into actionable outcomes for stakeholders. Your responsibilities include managing and optimizing the Horizon platform and related systems to empower teams in executing drug development projects with precision and agility. Additionally, you will champion the adoption of best practices in project management and collaborate with Biomedical Research (BR) to unlock synergies. Key Responsibilities: - Maintain and optimize the PPM platform and related project management systems to ensure robust operational capabilities for Development. - Act as the primary contact for the PPM/Horizon user community, offering expert guidance on Development Plans setup and management to meet governance and project management requirements. - Establish and enhance centralized project management processes, ensuring alignment with organizational standards and best practices. - Design and implement quality checks to ensure adherence to approved procedures and support data integrity in project plans and processes. - Collaborate with line functions and cross-divisional teams to drive initiatives that enhance data quality, process consistency, and operational efficiency. - Gather and address user feedback to enhance PPM/Horizon usability and contribute to the Horizon training strategy to promote best practices and cross-functional planning. - Support portfolio governance by recording IMB/Board decisions in Horizon and ensuring consistent execution of governance processes. - Contribute to project and portfolio reporting strategies, aiding in the development and implementation of PPM reports for senior management and Development Leadership Team reporting needs. Qua

As a Senior Associate, Healthcare Systems Implementation Consultant at RSM, you will be a part of the National Healthcare Consulting practice, contributing to all aspects of systems implementation life cycle related to integrating leading healthcare IT applications. Your role will involve defining customer requirements, system configuration, testing, training, and go-live support. Additionally, you will support strategic IT projects such as IT systems assessments, software selections, and roadmap development. You will collaborate with a multi-disciplined project team, working closely with consulting and client team members. Responsibilities: - Implement leading packaged software solutions designed for healthcare business and management processes, regulatory requirements, and other business needs like Epic, Cerner, and Solventum (3M) solutions. - Deploy innovative healthcare industry-specific solutions. - Assess current state workflow and ensure proposed future state aligns with project objectives. - Identify, assess, and solve complex business integration problems, requiring an in-depth evaluation of variable factors. - Collaborate with clients to configure, test, and validate the software application environment. - Contribute to IT systems assessments and software selection projects. - Train client personnel on new processes/systems. - Travel as needed, with the possibility of international travel to support system implementation efforts. Basic Qualifications: - Bachelor's degree in Computer Science, Health Information Management, or a related program. - Minimum of four years" experience in systems implementation projects and assessments. - Direct experience with software implementation in a healthcare setting. - Prior consulting experience. - Experience with leading electronic health records systems such as Epic and Cerner. - Experience with Clinical Coding and Clinical Documentation (e.g., Solventum (3M) 360 Encompass) is advantageous. - Experience with Patient Engagement and CRM solutions is a plus. RSM offers a competitive benefits and compensation package to all employees. The company values work-life balance, providing flexibility in your schedule to serve clients while managing life's demands. For more information on total rewards, visit https://rsmus.com/careers/india.html. At RSM, we are committed to equal opportunity and reasonable accommodation for individuals with disabilities. If you require accommodation during the recruitment process or employment/partnership, please email careers@rsmus.com to request assistance.,

As a Data Scientist at Novartis, you will have the opportunity to understand complex and critical business problems from various stakeholders and business functions. You will formulate an integrated analytical approach to mine data sources, employ statistical methods, and utilize machine learning algorithms to contribute to solving unmet medical needs, discover actionable insights, and automate processes for reducing effort and time for repeated use. Your role will involve managing the definition, implementation, and adherence to the overall data lifecycle of enterprise data, ensuring the availability of useful, clean, and accurate data throughout its useful lifecycle. Additionally, you will need to have high agility to work across various business domains. **Key Responsibilities:** - Innovate by transforming the way problems are solved using effective data management, Data Science, and Artificial Intelligence. - Articulate solutions/recommendations to business users. - Provide pathways to manage data effectively for analytical uses. - Present analytical content concisely and effectively to non-technical audiences and influence non-analytical business leaders to drive major strategic decisions based on analytical inputs. - Collaborate with internal stakeholders, external partners, institutions, and cross-functional teams to solve critical business problems and propose operational efficiencies and innovative approaches. - Evaluate the need for technology and novel scientific software, visualization tools, and new computation approaches to increase efficiency and quality of Novartis data sciences practices. - Identify research articles, reproduce/apply methodology to Novartis business problems, and contribute to cross-industry work streams in external relevant working groups. - Ensure exemplary communication with all stakeholders, including senior business leaders. - Contribute to the development of Novartis data management and data science capabilities. **Qualifications Required:** - Work Experience: 10+ years of relevant experience in Data Science. - Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategy, Data Visualization, Machine Learning (ML), Master Data Management, Python (Programming Language), R (Programming Language), Statistical Analysis. If managing a team, you will be expected to empower the team, provide guidance and coaching with limited guidance from more senior managers. Additionally, you will be responsible for the reporting of technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt. **Why Novartis:** Novartis is committed to reimagine medicine to improve and extend people's lives, striving to become the most valued and trusted medicines company in the world. By joining Novartis, you will be part of a mission-driven organization where associates are the driving force behind reaching ambitious goals. For more information on benefits and rewards at Novartis, please refer to the Novartis Life Handbook: [Novartis Life Handbook](https://www.novartis.com/careers/benefits-rewards) **Diversity and Inclusion:** Novartis is dedicated to building an outstanding, inclusive work environment with diverse teams that are representative of the patients and communities they serve. **Accessibility and Accommodation:** Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact [email protected] with details of your request and the job requisition number. Join the Novartis Network to stay connected and learn about suitable career opportunities: [Novartis Network](https://talentnetwork.novartis.com/network),

As a Digital Analyst at Novartis, you will play a crucial role in analyzing digital data, deriving insights, and optimizing digital marketing strategies to enhance business growth. Working closely with marketing teams, data scientists, and digital specialists, you will be responsible for measuring digital performance, identifying trends, and improving overall digital experiences. This position offers you the opportunity to leverage your analytical skills and contribute to the digital transformation of a leading global healthcare company. **Responsibilities:** - Conduct detailed analysis of digital data across various channels like websites, mobile apps, and social media platforms to uncover valuable insights, trends, and growth opportunities. - Collaborate with cross-functional teams to establish digital performance metrics, KPIs, and success criteria, ensuring proper tracking and data collection procedures are in place. - Utilize web analytics tools such as Google Analytics and Adobe Analytics to measure, track, and report on digital performance metrics, identifying areas for enhancement. - Develop and maintain dashboards and reports that offer actionable insights and visualizations to stakeholders. - Perform competitive analysis and benchmarking to recognize best practices and emerging trends in digital marketing. - Work with data scientists and digital specialists to implement data-driven marketing strategies and optimize digital touchpoints. - Stay updated on industry trends, digital analytics methodologies, and emerging technologies to drive innovation and improve digital capabilities. - Assist in creating and maintaining digital analytics frameworks, processes, and tools to ensure data accuracy, automation, and scalability. **Qualifications:** - Bachelor's degree in computer science, Marketing, Statistics, or a related field. A Master's degree is considered a plus. - 2-4 years of experience in digital analytics or a relevant analytical role. - Proficiency in digital analytics platforms like Google Analytics and Adobe Analytics, along with a solid understanding of digital marketing concepts. - Strong skills in using SQL, Python, or R for data manipulation and analysis. Experience with data visualization tools like Power BI is beneficial. - Possess an analytical mindset with the ability to translate data into actionable insights and recommendations. - Excellent communication and presentation skills to effectively convey complex concepts to non-technical stakeholders. - Strong attention to detail, prioritization skills, and ability to manage multiple projects while meeting deadlines. - Experience in the pharmaceutical or healthcare industry is advantageous. - Fluency in English is required, additional language skills are a bonus. If this opportunity aligns with your skills and interests, we encourage you to apply and be a part of our digital transformation journey at Novartis. If you require any reasonable accommodation due to a medical condition or disability during the recruitment process, please reach out to [email protected] with your request and contact information, mentioning the job requisition number. Novartis is dedicated to fostering an exceptional, inclusive work environment with diverse teams that reflect the patients and communities we serve.,

As a Specialist in Compliance & Analytics Reporting at our company, your role will involve providing technical support on specific MAP-associated systems under the guidance of the Manager. You will be responsible for implementing enhancements, resolving technical issues, and fulfilling ad hoc requests to support the US Business. Key Responsibilities: - Assist in technical enhancements and support for various internally-owned Microsoft Products and other systems such as Power BI, Power Automate, MS Forms, and Excel. - Support the implementation of new systems leveraging Microsoft Products approved by the US Business, and establish processes for managing the system and supporting users. - Compile and distribute requested reports or data to specific stakeholders on an ad hoc basis. - Act as the primary escalation point for any issues related to supported systems, offering tactical support, defining next steps, and ensuring the quality of deliverables. - Communicate complex data findings to non-technical stakeholders and provide problem-solving solutions. - Aid in the development of training materials for owned systems and attend trainings as a Subject Matter Expert when required. - Identify opportunities to enhance data quality, cleanliness, and democratization across owned and related platforms. Essential Requirements: - Bachelor's Degree in Computer Science or related field. - Preferred: Masters or Doctorate in Data Science or Data Analytics. - 3+ years of experience working with data and analytics in a highly regulated industry. - Certifications in Microsoft Power Products, including Power BI (PL300 required) and Power Automate (PL500 preferred). - Proficiency in DAX, R, Python, SQL, and SkyLearn coding languages. - Ability to structure, assess, and transform data using core functions in Excel. - Knowledge of the US Materials Approval Process and its significance in maintaining compliance and auditability. - Strong problem-solving and analytical skills. - Excellent communication and collaboration abilities. - Proactive approach to handling complex situations and problems. - Capacity to work under tight deadlines and manage multiple projects simultaneously. You will be part of a diverse and inclusive work environment at Novartis, committed to representing the patients and communities we serve. Novartis is dedicated to providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact diversityandincl.india@novartis.com with your request and contact information, mentioning the job requisition number. Novartis offers a rewarding work environment where you can collaborate with smart and passionate individuals to achieve breakthroughs that impact patients" lives. If you are ready to contribute to creating a brighter future, we welcome you to join our team. Visit our website to learn more: https://www.novartis.com/about/strategy/people-and-culture,

As a talented and motivated associate joining the Novartis Manufacturing IT team, you will have the exciting opportunity to work with the latest technologies, collaborate with a top-performing team, and be surrounded by highly skilled professionals. The location for this role can be in Barcelona, Hyderabad, or Ljubljana, with a requirement of being in the office for 12 days per month. ### Role Overview: You will be responsible for various key activities including system installation and configuration, validation, vendor collaboration, integration and digitalization, continuous improvement, successful implementation, compliance with validation protocols and regulatory requirements, stable operations and system uptime, and user satisfaction. ### Key Responsibilities: - Perform system installation and configuration of the MES software in close collaboration with vendors and IT teams. - Develop and execute validation protocols to verify system functionality and compliance with regulatory standards. - Collaborate with vendors to align system capabilities with manufacturing processes and manage the procurement process. - Integrate solutions into Novartis ecosystem ensuring data exchange per business requirements. - Monitor and evaluate system performance for optimization and translate business requirements into technical solutions. - Ensure successful implementation of the Manufacturing Execution System within project timelines, budget, and quality standards. - Validate system functionality and compliance with regulatory standards. - Maintain stable operations of the MES system with minimal downtime and interruptions. - Gather feedback from end-users to evaluate satisfaction with the MES system. ### Qualifications Required: - Bachelor's degree in computer science, engineering, or information technology. - Experience in MES systems. - Fluent English (written and verbal). - Digital and Tech savvy. Novartis is dedicated to fostering an inclusive work environment and diverse teams that represent the patients and communities they serve. If you need accommodation during the recruitment process due to a medical condition or disability, please reach out to the provided contact information. To learn more about Novartis and explore career opportunities, you can join the Novartis Network [here](https://talentnetwork.novartis.com/network).,

As a PMR Manager at Novartis, your role will involve supporting decision-making across the organization by designing innovative research approaches to answer key business questions and leading the development and execution of primary market research. You will be responsible for evaluating brands" performance and market trends using innovative statistical analysis techniques and ensuring tight alignment with global brand teams and country insights teams. **Key Responsibilities:** - Drive innovation and capability building to enhance process efficiency and value of Insights - Influence senior leaders at Novartis with your strong functional leadership skills - Lead experimentation and adoption of innovative PMR solutions globally - Monitor execution of PMR projects to support brand strategy performance and growth - Design and execute primary market research to deliver insights to brand teams - Establish expectations and approaches to understand and impact patient journeys - Foster a continuous improvement mindset within the team regarding data analysis - Plan and design market research analyses based on a sound understanding of research tools and techniques - Provide effective guidance for study planning and research material design - Input and guide report structure to illustrate complex analysis in a user-friendly manner - Implement studies on local, regional, and global levels - Design and implement new statistical methodologies to enhance research practices - Assist in achieving financial targets for PMR - Meet KPIs tied to performance for overall financial and department success **Essential Requirements:** - 7+ years of experience in market research or specialist agencies - Experience managing multi-methodology market research projects across multiple markets - Ability to work across regions within a commercial, primary market research team - Strong project management skills including scoping, defining deliverables, and business case development - Strong business acumen with budget and P&L management experience - Experience in remote relationships and offshore capability delivery - Preferred: Knowledge of disease areas within the Pharma sector and strong leadership and communication skills - University degree in business, statistics/mathematics, medicine, sciences, health economics, sociology, or psychology As part of Novartis, you will be contributing to building an outstanding, inclusive work environment and diverse teams that represent the patients and communities the company serves. Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact [email protected] with your request. Join the Novartis network to explore suitable career opportunities and benefits that support your personal and professional growth. Novartis offers a community of smart, passionate individuals collaborating to achieve breakthroughs that change patients" lives. Visit https://www.novartis.com/about/strategy/people-and-culture for more information.,

Job Description: As a Regulatory Affairs - CMC Specialist at Novartis, you will be responsible for activities related to chemistry, manufacturing, and control (CMC) for regulatory submissions to Health Authorities. Your role will involve formulating and leading global CMC regulatory strategy, authoring high-quality CMC documentation, and interacting with Health Authorities to support product launches. Key Responsibilities: - Lead global CMC regulatory strategy, focusing on innovation while ensuring regulatory compliance - Manage all global CMC submission activities for assigned projects/products - Identify required documentation for global submissions and negotiate delivery of approved technical documents - Author and review CMC documentation for Health Authority submission - Ensure technical congruency, regulatory compliance, and timely submission - Prepare CMC Risk Management Assessments, contingency plans, and escalate issues as needed - Initiate and lead Health Authority interactions and negotiations - Report technical complaints, adverse events, and distribute marketing samples as required Qualifications Required: - Minimum of 8+ years in Regulatory Affairs-CMC - Proven track record in HA negotiations and strategic vision development - Ability to work in a cross-functional environment and strong project management skills - Highly committed, team-oriented, with strong matrix leadership - Ability to recognize regulatory issues, conduct risk assessments, and overcome hurdles - Postgraduate in Pharmacy, Chemistry, Biochemistry, Biotechnology or equivalent - Ability to travel and represent the organization Additional Details: Novartis is committed to diversity and inclusion, creating an outstanding work environment and diverse teams. The company provides reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact diversityandincl.india@novartis.com. Why Novartis: Novartis is dedicated to helping patients and communities through innovative science and a community of passionate individuals. Join Novartis to collaborate, support, and inspire breakthroughs that change patients" lives. Learn more at https://www.novartis.com/about/strategy/people-and-culture. Join Our Novartis Network: If this role is not suitable for you, sign up for Novartis" talent community to stay connected and learn about career opportunities. Visit https://talentnetwork.novartis.com/network. Benefits and Rewards: Explore the handbook to discover how Novartis helps employees thrive personally and professionally. Visit https://www.novartis.com/careers/benefits-rewards.,

Role Overview: As part of Novartis, you will play a crucial role in driving the execution of the company's ambition to leverage data as a strategic asset for actionable insights. This role is focused on designing and implementing Data Governance processes and Data Operating Model within the Operations Data Domain, in collaboration with the Enterprise Data Owner and team members. Your responsibilities will include establishing and developing data capabilities at Novartis and leading the implementation within the LDC scope. Key Responsibilities: - Implement data principles, data governance framework, data ownership, and data operations within specific designated Operations Data area(s). - Ensure adoption of FAIR (Findable, Accessible, Interoperable, Reusable) data solutions across the legacy landscape. - Gather and implement data requirements from Business Function, Operations EDO, and other dependent projects/programs. - Validate data ideas, concepts, and features with internal stakeholders at all levels of the business. - Improve data literacy across the business through training and education. - Identify data issues proactively, work with stakeholders to implement corrective measures, and continuously improve data quality and integrity. - Drive the transition into new ways of working as defined by the Enterprise Operating model. - Manage data quality definition for the assigned data within the Operations Data team. Qualification Required: - Education: Master's university degree or higher. - Experience: Minimum 5 years of experience in country and global Operations roles, with experience in data, system configuration workstreams, ERP/systems implementations, and global business transformations. SAP MM experience is mandatory. - Languages: Proficiency in English required, additional languages preferred. Additional Company Details: Novartis is dedicated to helping people with diseases and their families through innovative science and a community of passionate individuals. They value collaboration, support, and inspiration to achieve breakthroughs that positively impact patients" lives. If you are ready to contribute to creating a brighter future, Novartis offers a network of career opportunities and benefits to support your personal and professional growth. Note: For any accommodation due to disabilities during the recruitment process, please contact [email protected] Novartis is committed to fostering an inclusive work environment and diverse teams that reflect the patients and communities they serve.,

Role Overview: Working at Bristol Myers Squibb is not your usual job. You will be part of uniquely interesting work that happens every day, across various departments, from optimizing production lines to the latest breakthroughs in cell therapy. Your work will have a direct impact on transforming the lives of patients and shaping your career. Bristol Myers Squibb offers opportunities uncommon in scale and scope, allowing you to grow and thrive in a high-achieving team environment. Key Responsibilities: - Work collaboratively with audit teams to execute financial, operational, compliance, and integrated-IT audits. - Conduct planning activities to identify significant risks and develop appropriate risk-based audit procedures. - Research applicable policies, guidance, and regulations to drive assigned sections of the audit with high quality and within deadlines. - Interview key personnel to assess business processes and the strength of their control environments. - Identify value-added recommendations for management to enhance the adequacy, effectiveness, and efficiency of controls and related processes. - Lead meetings with various levels of management to communicate audit status, align on significant audit issues, and recommend corrective actions. - Prepare detailed audit documentation in accordance with BMS and the Institute of Internal Auditors (IIA) standards. - Prepare audit reports with concise audit observations to communicate identified issues and corrective actions effectively to key stakeholders. - Participate in trainings, departmental meetings, and projects as assigned. Qualifications Required: - BA/BS degree in Data Science, Computer Science, Information Systems, Accounting, Finance, or other business discipline. - Minimum of 4 years prior public accounting or internal audit experience in financial, operational, IT, or compliance auditing. - Knowledge of U.S. GAAP and IIA standards. - English fluency. - Strong verbal and written communication skills. - Proficiency with Excel, Word, PowerPoint. Experience with AI, data analytics, and visualization tools such as Tableau and ERPs. Additional Company Details: Bristol Myers Squibb recognizes the importance of balance and flexibility in the work environment. The company offers competitive benefits, services, and programs to support employees in pursuing their goals at work and in their personal lives. The company is committed to ensuring that individuals with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments, and ongoing support in their roles. If you are intrigued by a role that doesn't perfectly align with your resume, it is encouraged to apply as you could be one step away from work that will transform your life and career.,

As a Sourcing Manager R&D, Drug Development at Novartis, your primary responsibility will be to implement global category strategy at the local level or implement sourcing business plans for your area of responsibility. You will be directly deploying the global category strategy at the site level. **Key Responsibilities:** - Supervise the implementation of sourcing plans for the sub-category and deliver sub-category savings targets following engagement in the target setting process. - Provide input into the overall Category segmentation and identification of key supplier relationships or directly control purchases with respect to supplier choice, timing, and commercial conditions on a local basis. - Manage strategic sub-category supplier relationships and implement consistent key performance indicators for the sub-category, reporting on suppliers" performance. - Collect supplier information and feedback from Divisions, countries, sites, Category teams, and Business Partners, delivering Procurement Balanced Scorecard metrics for the relevant sub-category. - Build, apply, complete, and review major contracts for the sub-category, ensuring negotiated contracts are clearly communicated and consistently applied. **Qualifications Required:** - University/Advanced degree with a strong preference in Business, Lifesciences, Pharmaceutical sciences, or a Scientific field with proficient written and spoken English skills. - 7+ years of experience in Global Strategic Procurement or related experience within the Pharmaceutical industry, preferably in category management, supplier management, or a related area, with a strong focus in the Comparator and Clinical Supply domain. As a part of Novartis, you will be contributing to the purpose of reimagining medicine to improve and extend people's lives. The vision is to become the most valued and trusted medicines company globally, driven by the dedication of the associates. Join this mission to create a brighter future together. Novartis is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require accommodation during the recruitment process, please reach out to [email protected] with your request and contact information, mentioning the job requisition number. Join the Novartis Network to stay connected and learn about suitable career opportunities as they arise, contributing to a diverse, inclusive work environment that represents the patients and communities served by Novartis.,

As a Regulatory Affairs-CMC Specialist at Novartis, your role will involve handling regulatory activities related to chemistry, manufacturing, and control (CMC). You will be responsible for preparing and publishing REG CMC documentation for submissions to Health Authorities. Additionally, you will interact with Health Authorities on REG CMC questions to support new product launches and post-market activities. Key Responsibilities: - Formulate and lead global CMC regulatory strategy, focusing on innovation while ensuring regulatory compliance. - Lead and oversee all global CMC submission activities for assigned projects/products. - Identify required documentation for global submissions, address content, quality, and timeline issues, and ensure timely delivery of approved technical documents. - Author and review high-quality CMC documentation for Health Authority submission following global regulatory strategies and guidelines. - Ensure technical congruency, regulatory compliance, and meet e-publishing requirements within agreed timelines. - Prepare and communicate CMC Risk Management Assessments, contingency plans, and lessons learned on major submissions. - Initiate and lead interactions and negotiations with Health Authorities, preparing briefing materials and risk mitigation plans. - Report technical complaints, adverse events, and special case scenarios related to Novartis products promptly. - Distribute marketing samples where applicable. Qualifications Required: - Minimum of 8+ years of experience in Regulatory Affairs-CMC. - Proven track record in HA negotiations and the ability to develop and communicate strategic visions. - Expertise in project management and working in cross-functional environments. - Strong matrix leadership skills and commitment to teamwork. - Early recognition of regulatory issues, sound risk assessment, and problem-solving abilities. - Postgraduate degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, or equivalent. Desirable Qualifications: - Experience in Regulatory Affairs-CMC authoring. Novartis is committed to fostering diversity and inclusion in the workplace, aiming to create an inclusive work environment and diverse teams that represent the patients and communities they serve. If you require any accommodations due to a medical condition or disability during the recruitment process or while performing job functions, please reach out to diversityandincl.india@novartis.com with your request and contact information. Novartis values collaboration, support, and inspiration among its employees to achieve breakthroughs that positively impact patients" lives. Join the Novartis community to contribute to a brighter future together and explore career opportunities within the network. For more information on benefits and rewards offered by Novartis, please refer to the handbook: https://www.novartis.com/careers/benefits-rewards.,

As a Team Lead-Content at Novartis, you will be responsible for managing the functional and operational aspects of the content team. Your role will involve ensuring the timely delivery of high-quality, compliant, and scientifically accurate content across multiple therapy areas, brands, and channels. You will oversee daily operations, project allocation, and workload distribution to optimize resource allocation and drive efficient execution. Additionally, you will plan and execute multiple projects, track project progress, identify and document risks and issues, and share updates with stakeholders to ensure the timely delivery of promotional materials. Your role will also include maintaining visibility and tracking of current and upcoming projects. Key Responsibilities: - Support, plan, execute, and manage assigned projects in collaboration with stakeholders and cross-functional teams. - Deliver marketing materials with accuracy, clarity, and consistency in alignment with regulatory and company policies. - Evaluate resource requirements, timelines, and logistics for projects, assign tasks, and coordinate with involved teams for project execution. - Guide the team to ensure efficient and effective project execution, fostering a collaborative work environment and providing mentorship and support. - Track team performance and productivity, conduct regular performance reviews, and provide feedback to team members. - Develop standardized workflows, templates, and review mechanisms, manage dependencies with other teams, and drive continuous improvement. - Act as a liaison for content development queries, escalations, and interdependencies. - Track and report on content pipeline, productivity metrics, and quality KPIs. - Implement content quality control measures and drive best practices in content reuse and repurposing across platforms. - Deliver projects according to Novartis Brand standards and support leadership in driving initiatives. Qualifications Required: - Advanced degree (MSc/PhD/PharmD/MD) in Life Sciences, Pharmacy, or related discipline. - 10+ years of experience in medical/scientific content development, with 3+ years in a leadership or supervisory role. - Deep understanding of pharma/healthcare regulations, compliance (FDA), and label update processes, with a strong track record of managing content across global teams and platforms. About Novartis: Novartis is committed to building an outstanding, inclusive work environment and diverse teams that are representative of the patients and communities served. The company also provides accessibility and accommodation for individuals with disabilities to ensure equal opportunities during the recruitment process. If you are passionate about making a difference in patients" lives through innovative science and collaborative teamwork, Novartis offers a supportive community where you can thrive both personally and professionally. Join the Novartis network to explore career opportunities and be part of a brighter future together. Please refer to the company's official website for more information on benefits, rewards, and career development opportunities.,

Role Overview: As an Associate Director Medical Information Group Lead at Novartis, you will be accountable for managing and leading a Medical Information delivery team to produce high-quality medical information documents and responses. You will play a key role in driving functional excellence, stakeholder management, and ensuring compliance with all relevant internal SOPs/guidelines and external regulatory requirements. Key Responsibilities: - Responsible for the performance of the assigned Medical Information team to deliver as designed with quality, timeliness, and in a compliant manner. - Track progress, identify improvement opportunities, and share best practices across the Medical Information delivery teams. - Co-ordinate capacity and workforce planning for assigned programs and deliverables to meet business needs. - Drive functional excellence and consistency in delivery. - Manage stakeholder expectations, act as an escalation point for issues, and ensure effective resolutions. - Support operational governance and business planning with standardization of processes. - Recruit and retain talent, manage performance, and develop associates. - Develop high performing teams in a constructive culture and ensure compliance and inspection/audit readiness. Qualification Required: - Advanced degree (PhD, PharmD, MD) in life science/healthcare or relevant experience. Desirable: MBA - More than 10 years of pharmaceutical industry experience in Medical Information. - Equal to or more than 3 years of people management experience. - Proven track record in customer delivery environments and experience with the development of MI services in shared service centers. - Deep understanding of good practices in medical enquiry management, medical information writing, and medical content review. - Experience with developing, implementing, and maintaining processes that adhere to company, industry, and HA requirements. - Superior people management skills with demonstrated positive leadership, innovative, and collaborative behaviors. - Proven ability in interpersonal, communication, negotiation, and diplomacy skills. - Demonstrated influencing and leadership skills in an international matrixed environment. Additional Details: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities served. The company's purpose is to reimagine medicine to improve and extend people's lives, with a vision to become the most valued and trusted medicines company globally. Novartis values its associates who drive the company each day to reach its ambitions. To learn more about Novartis, you can visit: [https://www.novartis.com/about/strategy/people-and-culture](https://www.novartis.com/about/strategy/people-and-culture). Please note that Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process or for the essential functions of a position, you can reach out to [email protected] with your request and contact information, mentioning the job requisition number.,

As a Customer Service Manager in the hospital setting, your role will involve defining, setting, and auditing Customer Service standards within your work area. You will need to model high-level customer-focused behaviors and coach others to excel in customer care. Additionally, you will be responsible for managing Hospital patient administration processes, including medical records, to ensure efficiency and effectiveness, all while directing the team to achieve budgetary targets. Your key responsibilities will include: - Ensuring that all wards are cleaned to an acceptable standard, consistent with special requirements of kitchens and infection control policies. You will provide facilities that are clean, undamaged, and appropriate. - Selecting, appointing, retaining, and promoting the most appropriately qualified and experienced staff in conjunction with Human Resources. - Handling patient and attender grievances, complaints, and suggestions, taking measures to improve based on feedback within the hospital policies. - Establishing work and time plans for all staff in the department to maximize efficient use of staff time. - Providing continuous training and developing the knowledge and skills of staff. - Ensuring all staff in the team conduct themselves professionally, are well presented, and adhere to Company policy. - Coordinating with consultants for quality patient care and smooth departmental functioning. - Assessing staff performance levels and reviewing annual appraisals with Human Resources. - Managing annual leave entitlement to maintain appropriate staffing levels throughout the year. - Minimizing discharge processes through close coordination with all departments involved. - Overseeing Bio-medical waste management and ensuring Quality standards are in line with NABH guidelines. - Upholding ethical and moral practices, setting goals for best practices and quality assurance. - Providing feedback to management on customer/patient requirements/expectations by maintaining constant patient relations and conducting surveys. This is a full-time position with benefits such as leave encashment, paid sick time, and Provident Fund. The work location is in person. As a Customer Service Manager in the hospital setting, your role will involve defining, setting, and auditing Customer Service standards within your work area. You will need to model high-level customer-focused behaviors and coach others to excel in customer care. Additionally, you will be responsible for managing Hospital patient administration processes, including medical records, to ensure efficiency and effectiveness, all while directing the team to achieve budgetary targets. Your key responsibilities will include: - Ensuring that all wards are cleaned to an acceptable standard, consistent with special requirements of kitchens and infection control policies. You will provide facilities that are clean, undamaged, and appropriate. - Selecting, appointing, retaining, and promoting the most appropriately qualified and experienced staff in conjunction with Human Resources. - Handling patient and attender grievances, complaints, and suggestions, taking measures to improve based on feedback within the hospital policies. - Establishing work and time plans for all staff in the department to maximize efficient use of staff time. - Providing continuous training and developing the knowledge and skills of staff. - Ensuring all staff in the team conduct themselves professionally, are well presented, and adhere to Company policy. - Coordinating with consultants for quality patient care and smooth departmental functioning. - Assessing staff performance levels and reviewing annual appraisals with Human Resources. - Managing annual leave entitlement to maintain appropriate staffing levels throughout the year. - Minimizing discharge processes through close coordination with all departments involved. - Overseeing Bio-medical waste management and ensuring Quality standards are in line with NABH guidelines. - Upholding ethical and moral practices, setting goals for best practices and quality assurance. - Providing feedback to management on customer/patient requirements/expectations by maintaining constant patient relations and conducting surveys. This is a full-time position with benefits such as leave encashment, paid sick time, and Provident Fund. The work location is in person.

As a Team Lead-Content at Novartis, you will be responsible for managing the functional and operational aspects of the content team. Your role will involve ensuring timely delivery of high-quality, compliant, and scientifically accurate content across multiple therapy areas, brands, and channels. You will oversee daily operations, project allocation, and workload distribution to optimize resource allocation and drive efficient execution. Additionally, you will be planning and executing multiple projects, tracking project progress, identifying and documenting risks and issues, and sharing updates with stakeholders to ensure the timely delivery of promotional materials. It will also be your responsibility to maintain visibility and tracking of current and upcoming projects. Key Responsibilities: - Support, plan, execute, and manage assigned projects in collaboration with stakeholders and cross-functional teams. - Deliver assigned marketing materials with accuracy, clarity, and consistency in alignment with regulatory and company policies. - Evaluate resource requirements, timelines, and logistics for projects. Assign tasks and coordinate with involved teams for project execution. - Oversee and guide the team for efficient project execution, fostering a collaborative work environment and providing mentorship and support. - Track team performance and productivity, conduct regular performance reviews, and provide feedback. Prepare and present reports on team progress and project outcomes to senior management. - Develop standardized workflows, templates, and review mechanisms. Manage dependencies with creative, digital, and quality teams. - Identify process gaps, drive continuous improvement, and reduce cycle times. - Act as a liaison for content development queries, escalations, and interdependencies. - Track and report on content pipeline, productivity metrics, and quality KPIs. - Provide updates on capacity planning, risks, and mitigation measures. - Implement content quality control measures and drive best practices in content development. - Deliver projects as per Novartis Brand standards, maintaining compliance, quality, and production efficiency KPIs. Qualifications Required: - Advanced degree (MSc/PhD/PharmD/MD) in Life Sciences, Pharmacy, or related discipline. - 10+ years of experience in medical/scientific content development, with 3+ years in a leadership role. - Deep understanding of pharma/healthcare regulations, compliance, and label update processes. In addition to the above, Novartis is committed to diversity and inclusion in the workplace. The company also provides accessibility and accommodation to individuals with disabilities. If you require reasonable accommodation during the recruitment process, please reach out to diversityandincl.india@novartis.com. Join Novartis in their mission to help people with diseases and their families by collaborating with a community of smart, passionate individuals to achieve breakthroughs that change patients" lives. Visit https://www.novartis.com/about/strategy/people-and-culture to learn more about creating a brighter future together with Novartis. If this role is not the right fit for you, you can sign up to Novartis" talent community to stay connected and learn about suitable career opportunities as they arise: https://talentnetwork.novartis.com/network. For details on benefits and rewards offered by Novartis, refer to their handbook: https://www.novartis.com/careers/benefits-rewards.,

As a Software Developer at Endpoint, you will play a crucial role in programming the implementation of individual client projects. Your responsibilities will include: - Understanding the individual design requirements for a specific client implementation and creating any required custom development. - Being proficient in front and back-end development to make modifications and enhancements across all aspects of the system. - Collaborating with designers, project managers, and testing teams on application usability, features, and performance. - Converting requirements documents into robust technical solutions. - Managing projects from requirements to launch, including code review, testing, and deployment. - Promoting emerging technologies and integrating them intelligently into our product suite. Qualifications: - Bachelor's degree or equivalent and/or appropriate experience. Experience: - 2-8 years of experience with system design and development, particularly using C#, JavaScript, and SQL Server T-SQL. - Strong expertise in various technologies such as ASP.NET, MVC, EntityFramework, LINQ, IIS, RESTful WebServices, CSS, and JQuery. - Proficient in the generation and parsing of XML and JSON formatted files. Key Skills: - Strong attention to detail. - Excellent organizational and time management skills. - Good communication skills. - Attentive and active listening skills. Endpoint is an interactive response technology (IRT) systems and solutions provider dedicated to supporting the life sciences industry's success in clinical trials. With our proprietary PULSE platform, we optimize the supply chain, reduce operational costs, and ensure precise patient dosing. Headquartered in Raleigh-Durham, North Carolina, we have offices across the United States, Europe, and Asia. Please note that we may utilize artificial intelligence (AI) tools in parts of the hiring process to enhance our recruitment efforts. These tools aid our team in reviewing applications, analyzing resumes, and evaluating responses, but they do not replace human judgment. Ultimately, final hiring decisions are made by humans. If you have any queries regarding data processing, feel free to reach out to us.,

In this role, you will be responsible for working closely with ERP IT, Global Process owner, Global Supply Chain Logistics, and Business Champions to design, enhance, and support the deployment of the global transport management solution for Novartis. Your main responsibility will be to verify Novartis core business processes and system solutions within upcoming releases with local business Subject Matter Experts to ensure a proper go-live according to the LDC roadmap. Key Responsibilities: - Act as the responsible Solution Manager for Transport Management in collaboration with the GPO, Business Champions, and work stream lead - Coordinate and support project activities during the building of the solution by working with ERP IT to deliver solutions/functional design - Ensure that user requirements and functional specifications align with global/local processes - Align and integrate relevant processes of Transport Management and their system solutions within Logistics W&D - Execute business screening of IT solutions and testing of solutions - Help identify and update local & global SOPs and Working Instructions - Contribute to master data preparation for Screening, Testing, and cut-over - Support cutover and hypercare phases for proper go-live in countries - Establish or update business standard operating procedures - Review and adopt training material and working instructions - Secure business reporting requirements in Transport Management with the Reporting and Analytics team Qualifications Required: - Experience in working in Transport Management/Logistics, ideally with SAP transport management in combination with iNet/Alpega or experience in implementing SAP Transport Management S4/ECC - Successfully completed a university degree in supply chain management, logistics, information science, or related field - Highly organized with a strong orientation towards process/project management - Ability to work independently and in a structured manner - Positive and pro-active attitude - Flexibility to work in a fast-paced, changing environment - High degree of teamwork and quality orientation - Ability to operate in a global matrix environment - Project management experience and workload coordination within the team Desirable Requirements: - Business Scenario Analysis - Change Impact Assessment About Novartis: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities served. Join the Novartis Network to stay connected and learn about suitable career opportunities. Novartis is dedicated to reimagining medicine and improving lives, with a vision to become the most valued and trusted medicines company globally. For more details on benefits and rewards, refer to the Novartis Life Handbook. Location: Hyderabad, India Company/Legal Entity: IN10 (FCRS = IN010) Novartis Healthcare Private Limited Functional Area: Technical Operations Employment Type: Full-time, Regular Shift Work: No Accessibility and Accommodation: Novartis is committed to providing reasonable accommodation to individuals with disabilities. If you require accommodation during the recruitment process, please contact [email protected] with the job requisition number. In this role, you will be responsible for working closely with ERP IT, Global Process owner, Global Supply Chain Logistics, and Business Champions to design, enhance, and support the deployment of the global transport management solution for Novartis. Your main responsibility will be to verify Novartis core business processes and system solutions within upcoming releases with local business Subject Matter Experts to ensure a proper go-live according to the LDC roadmap. Key Responsibilities: - Act as the responsible Solution Manager for Transport Management in collaboration with the GPO, Business Champions, and work stream lead - Coordinate and support project activities during the building of the solution by working with ERP IT to deliver solutions/functional design - Ensure that user requirements and functional specifications align with global/local processes - Align and integrate relevant processes of Transport Management and their system solutions within Logistics W&D - Execute business screening of IT solutions and testing of solutions - Help identify and update local & global SOPs and Working Instructions - Contribute to master data preparation for Screening, Testing, and cut-over - Support cutover and hypercare phases for proper go-live in countries - Establish or update business standard operating procedures - Review and adopt training material and working instructions - Secure business reporting requirements in Transport Management with the Reporting and Analytics team Qualifications Required: - Experience in working in Transport Management/Logistics, ideally with SAP transport management in combination with iNet/Alpega or experience in implementing SAP Transport Management S4/ECC - S

As a Sourcer at Azurity Pharmaceuticals, you play a crucial role in identifying and engaging top-tier talent to meet the company's staffing needs. Your responsibilities include: - Utilizing various sourcing methods such as job boards, social media platforms, professional networks, and employee referrals to identify potential candidates. - Developing and maintaining a strong pipeline of qualified candidates for current and future hiring needs. - Conducting initial candidate screenings to assess their qualifications, skills, and cultural fit. - Building and nurturing relationships with passive and active candidates. - Collaborating with recruiters and hiring managers to understand job requirements and desired candidate profiles. - Maintaining accurate and up-to-date records of candidate interactions in the Applicant Tracking System (ATS). - Staying informed of market trends, industry insights, and best practices in talent sourcing and recruitment. - Assisting in employer branding initiatives to attract high-quality candidates. Preferred Qualifications & Pre-requisite Skills: - A bachelor's degree or equivalent work experience. - Proven experience in sourcing, preferably in pharma and shared services industries (especially R&D, Analytical Finance, IT, and Digital). - Familiarity with various sourcing tools and techniques, including Boolean searches. - Proficiency in Applicant Tracking Systems (ATS) and CRM tools. - Excellent communication and interpersonal skills. - Ability to work collaboratively in a team-oriented environment. - Experience sourcing candidates for niche or hard-to-fill roles. - Knowledge of recruitment metrics and analytics. - Familiarity with employer branding and candidate engagement strategies. Azurity Pharmaceuticals values inclusivity and is an Equal Opportunity Employer. The company focuses on developing and delivering dose-form innovations of established medicines for patients with unmet needs. Azurity encourages highly motivated individuals with dedication, integrity, and a creative spirit to thrive in the organization. Azurity leverages its integrated capabilities and vast partner network to expand its commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span various markets, including cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets. Join Azurity Pharmaceuticals to be part of shaping the future of India HR Shared Services and influencing a global organization while developing business and functional leadership skills. As a member of the HR Team, you will contribute to delivering the best science and commitment to quality in everything you do.,

Role Overview: Working at Bristol Myers Squibb is a unique and transformative experience where you will be involved in meaningful work that impacts the lives of patients. You will have opportunities to grow and thrive in a dynamic environment, working alongside high-achieving teams. As an Internal Audit Analyst III, you will play a crucial role in planning and executing risk-based audits to strengthen company processes and controls. Your work will involve interacting with senior management and enhancing your communication skills. Key Responsibilities: - Collaborate with audit teams to conduct financial, operational, compliance, and integrated-IT audits. - Conduct planning activities to identify significant risks and develop risk-based audit procedures. - Research policies, guidance, and regulations to drive audit sections with high quality and within deadlines. - Assist in data analytics AI projects and enhancements as required. - Interview key personnel to assess business processes and control environments. - Identify value-added recommendations to improve controls and related processes. - Lead meetings with management to communicate audit status and recommended corrective actions. - Prepare detailed audit documentation in accordance with BMS and IIA standards. - Create audit reports with clear, concise observations for key stakeholders. - Participate in trainings, meetings, and departmental projects as assigned. Qualifications Required: - Bachelor's degree in Data Science, Computer Science, Information Systems, Accounting, Finance, or a related field. - Minimum of 4 years of public accounting or internal audit experience. - Knowledge of U.S. GAAP and IIA standards. - Fluent in English with strong verbal and written communication skills. - Proficiency in Excel, Word, PowerPoint, AI, Data analytics, and visualization tools like Tableau. - Desired qualifications include an advanced degree, professional certifications, Big Four firm experience, and multilingual capabilities. Additional Company Details: Bristol Myers Squibb values balance and flexibility in the work environment, offering competitive benefits and programs to support employees in pursuing their goals at work and in their personal lives. The company is committed to inclusivity and diversity, empowering employees to make an impact on patient lives with shared values of passion, innovation, urgency, accountability, inclusion, and integrity. The company encourages individuals to apply even if their experience doesn't perfectly align with the job requirements, as transformative opportunities may be waiting. Please note that Bristol Myers Squibb has specific occupancy structures for employees based on role responsibilities, including onsite, hybrid, field-based, and remote roles. The company is dedicated to supporting individuals with disabilities through transparent recruitment processes and reasonable accommodations. BMS also prioritizes employee well-being by recommending full vaccination against Covid-19 and compliance with booster recommendations. Additionally, BMS complies with applicable data privacy policies and regulations in processing job applications.,