15 Ctm Jobs nearby Madurai

As a Sr. Product Integrator (ISG) in our organization, your role will involve integrating and managing product solutions, with a specific focus on RAVE and Veeva Vault for eTMF. Your responsibilities will play a crucial part in ensuring seamless operations and compliance within the company. Key Responsibilities: - Lead the integration of RAVE and Veeva Vault for eTMF to streamline document management processes. - Oversee the configuration and deployment of eTMF systems to ensure compliance with industry standards. - Provide technical expertise in managing and troubleshooting RAVE and Veeva Vault applications. - Collaborate with cross-functional teams to align product integration with business objectives. - Develop and implement strategies to enhance the efficiency of eTMF systems. - Monitor system performance and provide recommendations for improvements. - Ensure data integrity and security within the eTMF systems. - Conduct regular audits to maintain compliance with regulatory requirements. - Facilitate training sessions for team members on the use of RAVE and Veeva Vault. - Support research and development initiatives by providing technical insights. - Coordinate with stakeholders to gather requirements and deliver tailored solutions. - Document integration processes and maintain comprehensive records for future reference. - Contribute to the continuous improvement of product integration methodologies. Qualifications: - Possess a strong background in RAVE and Veeva Vault for eTMF with at least 5 years of experience. - Demonstrate expertise in managing electronic trial master files within a regulated environment. - Exhibit knowledge of research and development processes and their impact on product integration. - Have experience in hybrid work models adapting to both remote and on-site collaboration. - Show proficiency in troubleshooting and resolving technical issues related to eTMF systems.,

You are an experienced Veeva Configuration Specialist sought for a position in Chennai by Themesoft. Ideal candidates should possess Veeva certification. The role involves working with Veeva Vault Configurations, VQL, and related tasks in the life sciences sector. **Key Responsibilities:** - Acquire 5-12 years of experience in the life sciences sector with a focus on Veeva Vault Configurations for any Vault. - Execute implementation, support, and administration of Veeva Vault platform for various suites like CTMS, QMS, Safety, eTMF, etc. - Define and implement global business processes for safety. - Possess a thorough understanding of international regulations and associated business processes. - Evaluate the technical impact on current features and functionalities due to new releases and enhancements. - Provide guidance on business decisions and priorities for issue resolution strategies. **Qualifications Required:** - Veeva certification is preferred. - Proficiency in Veeva Vault Configurations and VQL. - Experience in the life science regulatory, QMS & clinical domain is advantageous. - Excellent communication, servant leadership, problem-solving, conflict-resolution, and organizational skills are desirable.,

Role Overview: As a Derivative Services - Bilateral Collateral Associate, you will be responsible for handling assigned tasks efficiently to ensure timely completion. You will support junior team members by acting as a go-to expert and assisting them with queries or problems. It is important to manage daily tasks effectively, recognize when assistance is needed, and escalate unresolved or high-risk issues promptly. Taking ownership of additional tasks or projects and completing them within agreed deadlines will be key in this role. Clear and prompt communication with clients and team members, following internal rules and procedures diligently, and sharing ideas for efficiency improvement will also be part of your responsibilities. Collaborating effectively with team members, building strong relationships with other teams and external partners, and escalating concerns to senior staff when necessary are essential aspects of this role. Key Responsibilities: - Handle assigned tasks and ensure timely completion - Support junior team members with queries or problems; act as a go-to expert - Manage daily tasks efficiently and recognize when to seek assistance - Resolve issues related to stock or cash differences; escalate unresolved or high-risk issues promptly - Take ownership of additional tasks or projects and complete them within agreed deadlines - Respond clearly and promptly to client and team queries - Follow all internal rules and procedures honestly and diligently to mitigate risks - Share ideas to enhance efficiency, reduce costs, and improve service quality - Collaborate effectively with team members to foster a positive work environment - Build and maintain strong relationships with other teams and external partners - Keep procedures updated and escalate any concerns to senior staff when necessary Qualifications Required: - Eagerness to continuously learn about transaction processes - Ability to plan and prioritize work effectively, even amid shifting priorities - Comprehensive knowledge of asset management from end to end - Strong understanding of global financial markets - Knowledge of derivatives and collateral management processes - Experience in trade operations across multiple asset classes (equities, fixed income, FX, money markets) - Familiarity with SWIFT messaging standards - Understanding of corporate actions, including income processing - Experience using Aladdin and related tools such as CTM, CLS, and SWIFT About UST: UST is a global digital transformation solutions provider that partners with clients from design to operation, embedding innovation and agility into their organizations. With over 30,000 employees in 30 countries, UST touches billions of lives through its boundless impact philosophy.,

As an Implementation Consultant at our company, your role will involve the following key responsibilities: - Responsible for creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. - Create wire-frames and mock-ups for Clinical reports. - Communicate with Clinical Data Management & Medical Reviewers to document the clinical reporting needs. - Stay up-to-date with all Saama product features and releases. - Analyze and understand current business processes, events, and flows in Clinical Trial Development. - Act as a Clinical Subject Matter Expert and provide Clinical Project Support. - Author and document business requirements, providing analytical support needed to translate requirements into solutions. - Create and maintain Data Mapping Specifications for Saama Data Review Model. - Incorporate feedback from customers, partners, and in-house teams on product. - Manage all aspects of projects related to implementation including guiding the client through release planning, managing communication, leading product implementation efforts, managing project team deliverables, documenting and reporting status and issues, identifying and managing risks, and acting as a client liaison. - Ensure a smooth transition of services from implementation to support. - Provide advanced analytical and reporting support to customers on various projects, solving complex problems and conducting complex analysis. - Support configuration and quality check with project teams to ensure the solution meets business objectives. - Help identify and define new sources of relevant data, analyze data, and make recommendations. - Support customer User Acceptance Testing (UAT) phase for any configuration change or issue triaging. - Understand and discuss the application and implications of changes to the process and relation to requirements. Desired Skills: - Experience in the Pharmaceutical industry is essential. - Good understanding of Clinical Systems such as EDC Systems (Medidata Rave, Veeva EDC, Oracle InForm, etc.), CTMS Systems (Siebel CTMS, Medidata CTMS, Veeva CTMS, etc.), IRT Systems (YPRIME, Parexel Clinphone, etc.), and LAB Systems (central Lab, local Labs, etc.). - Good experience in SQL. - Good understanding of the clinical trial domain, overall EDC study setup, and Clinical reporting. - Experience in building Clinical reports and dashboards. - Understanding of CDASH, SDTM, and ADAM standards. - Relevant degrees such as Bachelor's and Master's Degree in Healthcare, Computer Science, Technical, Engineering, Computer, Computer Engineering, Computer Programming - Bachelor's degree (BA) in computer science or equivalent work experience required. - 1-2 years of experience as a Product Owner. - Comfortable and familiar with the Agile Working Environment. - Experience working with all phases of Software Development Life Cycle (SDLC). - Familiarity with FDA regulations such as 21 CFR Part 11 and GxP is a bonus. - Experience working in the complete product life cycle of two or more products. - Technical knowledge including knowledge of Software Development and Web Development. - Experience with use and configuration of healthcare software applications (preferably clinical). As an Implementation Consultant at our company, your role will involve the following key responsibilities: - Responsible for creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. - Create wire-frames and mock-ups for Clinical reports. - Communicate with Clinical Data Management & Medical Reviewers to document the clinical reporting needs. - Stay up-to-date with all Saama product features and releases. - Analyze and understand current business processes, events, and flows in Clinical Trial Development. - Act as a Clinical Subject Matter Expert and provide Clinical Project Support. - Author and document business requirements, providing analytical support needed to translate requirements into solutions. - Create and maintain Data Mapping Specifications for Saama Data Review Model. - Incorporate feedback from customers, partners, and in-house teams on product. - Manage all aspects of projects related to implementation including guiding the client through release planning, managing communication, leading product implementation efforts, managing project team deliverables, documenting and reporting status and issues, identifying and managing risks, and acting as a client liaison. - Ensure a smooth transition of services from implementation to support. - Provide advanced analytical and reporting support to customers on various projects, solving complex problems and conducting complex analysis. - Support configuration and quality check with project teams to ensure the solution meets business objectives. - Help identify and define new sources of relevant data, analyze data, and make recommendations. - Support customer User Acceptance Testing (UAT) phase f

As a Veeva CTMS Configurator, your role will involve the following responsibilities: - Responsible for all Veeva Vault CTMS & TMF changes and implementation - Understand business requirements, and propose and design Tech solutions - Lead all Tech design and implementation meetings - Review work done by other configurators - Responsible for managing/performing deployments - Prepare deployment checklist, config specification and other tech documents - Responsible for environment management including Sandbox refresh, snapshots, etc. - Work with Veeva technical team for issues or new features related to Veeva Vault ClinOps product - Conduct tech impact assessment on current features and functionalities due to new release and enhancements - Guide business decisions and priorities when proposing resolution strategies for encountered issues Qualifications required for this role include: - Strong technical knowledge of Configurations in Veeva Vault Clinical Operations Suite mainly in Veeva CTMS & Veeva eTMF - Hands-On work experience on Veeva Vault platform configurations - Hands-On work experience on Veeva Vault CTMS & eTMF configurations - Knowledge of Clinical Trial data and processes across pharmaceuticals specifically as they relate to Clinical studies,

As an Implementation Consultant, you will be responsible for managing and assuming accountability for all aspects of projects related to implementation. Your key responsibilities will include: - Guiding the client through release planning in support of the overall project. - Managing communication throughout the team and stakeholders. - Leading product implementation efforts by coordinating with customers, product SME, and other teams. - Managing the quality of Implementation deliverables. - Documenting and reporting status on Risks, Issues, Actions, and Decisions. - Identifying, reporting, and managing risks; overcoming project obstacles. - Acting as a client liaison and representative by communicating client feedback to appropriate representatives and resolving outstanding issues on behalf of the client in a timely manner. - Understanding Clients clinical landscape and providing techno-functional solutions to evolving needs of the clients. - Analyzing and understanding current business processes, events, and flows in Clinical Trial Development and creating SOPs, Work instructions for the implementation/delivery team. - Ensuring a smooth transition of services from implementation to support. - Incorporating feedback and input from customers, partners, and in-house teams on saama product features. - Providing advanced analytical and reporting support to customers on various projects, solving complex problems, and/or conducting complex analysis. - Supporting configuration and quality check with project teams to ensure the solution will meet the business objectives of the requirements. - Helping identify and define new sources of relevant data, analyzing data, and making recommendations. - Understanding and discussing the application and implications of changes to the process and relation to requirements. Desired Skills: - Experience in the Lifesciences and Pharmaceutical industry is essential. - Good experience in SQL, APIs, and Integrations. - Good understanding of CDASH, SDTM, and ADAM standards. - Good understanding of EDC, CTMS, IRT, and LAB Systems. - Good understanding of the clinical trial domain, overall EDC study setup, and Clinical reporting. - Relevant degrees such as Bachelor's and Master's Degree in Healthcare, Computer Science, Technical, Engineering, Computer, Computer Engineering, Computer Programming - Bachelor's degree (BA) in computer science, or equivalent work experience required. - 3-5 years of experience as a Product Manager or 1-2 years of experience as a Product Owner. - Comfortable and familiar with the Agile Working Environment. - Experience working with all phases of SDLC. - Familiarity with FDA regulations such as 21 CFR Part 11 and GxP is a bonus. - Experience working in the complete product life cycle of two or more products. - Technical knowledge including knowledge of Software Development and Web Development. - Experience with use and configuration of healthcare software applications (preferably clinical).,

As a Data Analyst at Agilisium, your role will involve gathering, validating, and analyzing data from clinical, operational, and administrative systems. You will be responsible for building interactive reports and dashboards using tools like Power BI, Tableau, or similar platforms to present insights to leadership and stakeholders. Additionally, you will generate routine and ad hoc analytical outputs to support business decisions and performance reviews. Key Responsibilities: - Gather, validate, and analyze data from various systems - Build interactive reports and dashboards using Power BI, Tableau, or similar tools - Generate routine and ad hoc analytical outputs - Develop and monitor Key Performance Indicators (KPIs) and operational metrics - Identify performance trends and provide actionable insights - Support clinical operations and research teams by analyzing data related to study execution, patient enrollment, and protocol adherence - Partner with cross-functional teams to evaluate workflows and recommend process improvements Qualifications & Skills: - Bachelors or Masters degree in Life Sciences, Healthcare, Statistics, Data Analytics, or related discipline - 4-6 years of experience in data analytics within clinical operations, clinical research, or healthcare domains - Strong proficiency in data visualization tools such as Power BI, Tableau, or Qlik - Proficient in querying languages like SQL (Python or R is a plus) - Solid understanding of clinical operations processes, KPIs, and research data frameworks - Excellent analytical, problem-solving, and storytelling skills - Effective communicator with the ability to translate data insights into business actions - Ability to work independently with minimal supervision while collaborating across diverse teams - Deep expertise/experience with CTMS (not EDC) About Agilisium: Agilisium is the Life Sciences industry's premier Autonomous Agentic AI and Applied AI Services Company. They specialize in developing AI-engineered business processes that are autonomous, scalable, and purpose-built for Life Sciences. Agilisium has been recognized for their expertise and growth by organizations such as Everest Group, Inc. 5000, and AWS. They continue to invest in top-tier talent to drive innovation and impact across the Life Sciences value chain. Learn more: [www.agilisium.com](www.agilisium.com),

At Allucent, you will be a Sr. Clinical Research Associate Contractor (Sr.CRA) responsible for independently controlling and monitoring investigational sites, ensuring clinical studies are conducted according to trial protocols and in compliance with SOPs, regulations, and Good Clinical Practice principles. **Key Responsibilities:** - Govern highest quality standards for trial monitoring activities. - Conduct all study tasks in compliance with quality standards while maintaining efficiency. - Monitor activities at clinical study sites to ensure adherence to protocols, ICH, GCP, SOPs, and regulations. - Prepare and submit quality Site Visits Reports and Contact reports. - Maintain and update CTMS in compliance with SOPs. - Act as Document Owner for collected documents. - Provide functional assistance to project team members. - Liaise with project team members and Sponsor to track study progress. - Track and supervise collection of ongoing study data. - Represent Allucent in the global medical research community. - Identify potential problems and propose solutions. - Supervise generation of electronic tracking systems. - Support project oversight and management. - Support site staff in preparation for audits and inspections. - Report Quality Issues and support resolution of Corrective and Preventative Actions. **Qualifications Required:** - At least five years of clinical monitoring experience. - Relevant life science degree or medical/nursing background. - Strong understanding and application of Good Clinical Practices and SOPs. - Excellent written and verbal communication skills in English and local language. - Ability to work in a fast-paced environment. - Proficiency in Word, Excel, and PowerPoint. - Flexibility to travel an average of 8 days on site per month. - Understanding of medical terminology and clinical trials. - Strong organizational and time management skills. - Ability to establish effective working relationships and prioritize tasks. - Ability to work independently and in a team. At Allucent, you will receive a comprehensive benefits package, competitive salaries, departmental study/training budget, flexible working hours, remote/hybrid working options, leadership and mentoring opportunities, internal growth opportunities, financial rewards for employee referrals, access to online training programs, eligibility for recognition programs, and more.,

As a Clinical Project Manager, you will be responsible for overseeing clinical trials with a focus on interventional studies (Phase IIV). Your key responsibilities will include: - Directly managing and operationalizing clinical trial protocols into eSource/EDC workflows. - Managing end-to-end clinical trial processes such as start-up, site initiation, data collection, query management, and close-out. - Leading and mentoring CDM/clinical trial teams with a minimum of 5 years of people management experience. - Utilizing expertise in clinical trial systems like CTMS (CRIO preferred), eSource, and EDC platforms. - Working in pharmaceutical, biotechnology, or CRO environments across various therapeutic areas. - Ensuring compliance with regulatory requirements such as ICH-GCP, FDA, EMA, and HIPAA. - Handling system validation, change control, and maintaining audit/inspection readiness. You should have 10-15 years of experience in clinical trials, a strong background in managing interventional studies, and a thorough understanding of regulatory standards. Your experience in people management and expertise in clinical trial systems will be essential for success in this role.,

As the Data Management Manager at our company, your role involves overseeing the daily operations and strategic development of the clinical data management team. You will be responsible for ensuring the accuracy, integrity, and compliance of clinical trial data while providing leadership, training, and performance oversight to data specialists. The ideal candidate for this position is hands-on, with proven experience in clinical data entry, query resolution, coordinating complex interventional clinical trials, leadership skills, and a collaborative mindset. **Key Responsibilities:** - **Team Leadership & Oversight:** - Supervise, mentor, and support a team of Clinical Data Specialists, ensuring productivity, consistency, and adherence to quality standards. - Develop training plans, performance goals, and growth opportunities for team members. - Provide day-to-day guidance and troubleshooting support for the data team. - Manage team capacity, schedules, and workloads across studies and projects. - Promote collaboration and positive communication within the team and with cross-functional departments. - **Data Management & Quality Assurance:** - Perform quality control on source documentation in CTMS and EDC systems as well as data entry into various systems. - Review and resolve complex data discrepancies and queries to ensure accuracy and consistency with source documentation. - Participate in and oversee the implementation and adherence to protocols, CRF guidelines, and regulatory standards. - Verify that source documents adhere to ALCOA-C guidelines and ensure data entries are accurate and consistent with source documentation. - Identify the need for corrections and resolve data discrepancies or queries promptly and effectively. - Lead quality control measures and data validation processes to maintain high standards of data integrity. - **Process Development & Compliance:** - Lead the creation and continuous improvement of source documents, SOPs, data workflows, and training materials. - Lead collaboration with clinical operations, regulatory, and sponsor teams to ensure alignment and data quality across studies. - Identify process inefficiencies and propose solutions to enhance data workflow and team productivity. **Qualifications and Experience:** - Bachelors degree in life science, health science, or related field (preferred). - Minimum 7 - 10 years of combined experience as a lead/manager of clinical data management team and experience as a lead/manager as Clinical Research Coordinator of complex interventional clinical trials. - Strong working knowledge of CMTS CRIO and EDC systems such as RAVE, Veeva Vault, Clinical One, and Inform. - Thorough understanding of GCP, HIPAA, ALCOA-C, ICH guidelines, and clinical trial data standards. - Proven ability to manage and mentor a team while balancing hands-on tasks. - Excellent organizational, problem-solving, and communication skills. - Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). - Ability to manage multiple projects and deadlines in a fast-paced environment. This job is a full-time position with benefits including health insurance, internet reimbursement, leave encashment, life insurance, paid sick time, paid time off, provident fund, and work from home option. The work schedule is Monday to Friday in US shift timings with a performance bonus included.,

As an Integration Architect (ISG) at the company, you will play a crucial role in designing and implementing integration solutions for clinical operations. Your primary focus will be on Vault CTMS eTMF Medidata Rave and Rave Integration to ensure seamless data flow and system interoperability. **Responsibilities:** - Design and implement integration solutions for clinical operations to guarantee smooth data flow. - Collaborate with cross-functional teams to gather requirements and develop integration strategies. - Develop and maintain integration architecture using Vault CTMS eTMF and Medidata Rave. - Ensure system interoperability and data integrity across clinical operations platforms. - Provide technical expertise and support for integration-related issues and challenges. - Monitor integration processes and troubleshoot any issues to maintain system performance. - Optimize integration workflows to enhance efficiency and reduce operational costs. - Document integration processes and maintain comprehensive technical documentation. - Stay updated with the latest integration technologies and industry best practices. - Conduct regular reviews of integration solutions to ensure alignment with business objectives. - Work closely with stakeholders to understand their needs and provide tailored integration solutions. - Support the development and implementation of integration testing strategies. - Contribute to the continuous improvement of integration processes and methodologies. **Qualifications:** - Possess strong experience in Vault CTMS eTMF Medidata Rave and Rave Integration. - Demonstrate a deep understanding of clinical operations and related processes. - Have a proven track record of designing and implementing integration solutions. - Exhibit excellent problem-solving skills and attention to detail. - Show proficiency in documenting technical processes and maintaining records. - Display strong communication skills to collaborate with cross-functional teams. - Be adaptable to new technologies and willing to learn continuously.,

Role Overview: As a GeoSpatial Lead Analyst MAP, you will be responsible for leveraging geospatial data to drive strategic insights and decision-making within the organization, specifically focusing on Veeva CTMS. Your role will involve analyzing complex datasets to support business objectives. You will have the opportunity to work in a hybrid model, offering flexibility and collaboration opportunities. Key Responsibilities: - Analyze geospatial data to provide actionable insights that align with business goals. - Collaborate with cross-functional teams to integrate geospatial data into existing systems. - Develop and maintain geospatial databases to ensure data accuracy and accessibility. - Utilize Veeva CTMS to streamline data management processes and enhance operational efficiency. - Design and implement geospatial models to support strategic decision-making. - Provide technical expertise in geospatial analysis to support project teams. - Conduct data validation and quality checks to ensure data integrity. - Create detailed reports and visualizations to communicate findings to stakeholders. - Stay updated with the latest geospatial technologies and methodologies. - Support the development of geospatial strategies to drive business growth. - Facilitate workshops and training sessions to enhance team capabilities in geospatial analysis. - Ensure compliance with data privacy and security standards in all geospatial activities. - Contribute to the continuous improvement of geospatial processes and tools. Qualifications: - Possess a strong background in geospatial analysis with a focus on Veeva CTMS. - Demonstrate proficiency in data management and visualization tools. - Exhibit excellent problem-solving skills and attention to detail. - Have experience in a hybrid work environment balancing remote and in-office tasks. - Show ability to work collaboratively with diverse teams. - Display strong communication skills to effectively present complex data insights. - Hold a degree in Geography, Geospatial Science, or a related field. Certifications Required: - Veeva certification,

Role Overview: As a Trade Operations Securities and Repo professional with 2.5 to 4 years of experience, your main duties will involve ensuring all assigned tasks and transactions are completed on time, supporting junior team members, investigating and resolving issues related to stock or cash mismatches, taking ownership of additional tasks or projects, responding to queries in a professional manner, adhering strictly to internal policies and compliance guidelines, contributing to process improvement initiatives, building and maintaining strong working relationships, and ensuring procedural documentation is up to date. Key Responsibilities: - Ensure all assigned tasks and transactions are completed on time; follow up or escalate where necessary. - Support junior team members by answering queries and acting as a subject matter expert. - Investigate and resolve issues related to stock or cash mismatches, escalating unresolved or high-risk discrepancies as per escalation policies. - Take ownership of additional tasks or projects and ensure timely and accurate completion. - Respond to internal and external queries in a clear, professional, and timely manner. - Adhere strictly to internal policies, procedures, and compliance guidelines to minimize operational risk. - Contribute to process improvement initiatives that enhance efficiency, reduce cost, or elevate service quality. - Build and maintain strong working relationships with internal departments, portfolio managers, dealers, and external partners. - Ensure procedural documentation is kept up to date and escalate any gaps or concerns to senior management. Qualifications Required: - Proficiency in using Aladdin, CTM, CLS, and SWIFT systems. - Strong understanding of global financial markets. - Experience with derivatives and collateral management processes. - Proven background in trade operations across asset classes (equities, fixed income, FX, money markets). - Familiarity with SWIFT messaging protocols. - Knowledge of corporate actions and income processing. - Understanding of risks inherent in the transaction and asset servicing lifecycle. Additional Details of the Company: N/A,

As a Regulatory Specialist, you will be responsible for the following key responsibilities: - Bachelor's degree in Life Sciences, Clinical Research, Science, Healthcare Administration, or a related field. - 25 years of regulatory experience in clinical research or pharmaceutical environments. - CITI certifications (GCP, HSC, RCR, COI, IPS, IATA, ICH, CRC) required within two weeks of hire; training will be provided. - Familiarity with IRB submissions, study start-up activities, and regulatory document maintenance. - Proficiency with CRIO (Clinical Research IO) or similar electronic platforms used for eISF and study documentation. - Experience with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) platforms, and eISF systems. - Working knowledge of FDA, OHRP, and ICH-GCP guidelines. - Prior experience supporting sponsor or FDA audits/inspections. - Strong organizational, communication, and time-management skills. - Ability to work independently and manage multiple priorities. You will need to have a Bachelor's degree in a relevant field and at least 7 years of experience in regulatory affairs within clinical research or pharmaceutical settings. Additionally, you must possess CITI certifications and have proficiency in various electronic platforms used for study documentation. Your familiarity with regulatory guidelines and ability to support audits will be crucial in this role. Strong organizational and communication skills are essential for success, along with the ability to work independently and prioritize tasks effectively.,

As a Veeva Config Specialist, your role will primarily involve focusing on Veeva Vault Configurations in the life sciences sector. Your key responsibilities will include: - Having 5-8 years of experience in the life sciences sector, with a strong emphasis on Veeva Vault Configurations for any Vault. - Proficiency in implementing, supporting, and administering the Veeva Vault platform, including suites such as CTMS, QMS, Safety, and eTMF. - Defining and implementing global business processes for safety, demonstrating the ability to navigate international regulations and associated business processes. - Conducting tech impact assessments on current features and functionalities in response to new releases and enhancements. - Guiding business decisions and priorities by proposing resolution strategies for encountered issues. It would be beneficial if you also have experience in Life Science Regulatory, QMS & Clinical domain and business processes, along with excellent communication and servant leadership skills. Problem-solving, conflict-resolution ability, and outstanding organizational skills are key attributes for this role. Additionally, holding a Veeva Vault Platform admin certification would be a plus. For any additional details about the company, please refer to the Job Description provided.,