365 Scientific Presentation Jobs in Arcot

As a Medical Writer at Novartis, your role involves writing, supporting, and managing projects to prepare high-quality medical and scientific communications. This includes conducting literature reviews, creating abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or internal medical and clinical team meetings. Your key responsibilities will include: - Preparing literature reviews, abstracts, posters, slide sets, and complex manuscripts using data from various sources such as clinical study reports and patient profiles. - Performing quality control checks and proofreading deliverables to ensure they meet customer expectations. - Managing multiple projects simultaneously, focusing on up to two brands at a time. - Obtaining feedback from customers and implementing customer management tactics. - Following Novartis specifications for documentation and tracking clinical trial milestones for assigned projects. - Maintaining records for all projects, including archiving and ensuring audit, SOP, and training compliance. - Training new team members and colleagues when required, in addition to performing any other assigned tasks. The minimum requirements for this role are: - Science degree or equivalent, B.Sc./equivalent with 8 years of Clinical Research (CR) experience, or M.Sc./M.Pharm +6 years of clinical research (CR) experience. - Desired qualifications include a Doctoral Degree or a Qualification in Medical Sciences (MBBS/MD/equivalent). - Alternatively, a PhD + 4 years of CR experience, MBBS/equivalent + 4 years of CR experience, or MD + 2 years of CR experience. Novartis is dedicated to reimagining medicine to improve and extend people's lives. By becoming a part of Novartis, you will contribute to our vision of becoming the most valued and trusted medicines company globally. If you are ready to join a mission-driven organization with a commitment to diversity and inclusion, consider applying to be a Medical Writer at Novartis. To learn more about our company culture and career opportunities, visit: [Novartis People and Culture](https://www.novartis.com/about/strategy/people-and-culture). Explore our benefits and rewards in the Novartis Life Handbook: [Novartis Benefits and Rewards](https://www.novartis.com/careers/benefits-rewards). Join the Novartis Network to stay connected and receive updates on future career opportunities: [Novartis Network](https://talentnetwork.novartis.com/network). As a Medical Writer at Novartis, your role involves writing, supporting, and managing projects to prepare high-quality medical and scientific communications. This includes conducting literature reviews, creating abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or internal medical and clinical team meetings. Your key responsibilities will include: - Preparing literature reviews, abstracts, posters, slide sets, and complex manuscripts using data from various sources such as clinical study reports and patient profiles. - Performing quality control checks and proofreading deliverables to ensure they meet customer expectations. - Managing multiple projects simultaneously, focusing on up to two brands at a time. - Obtaining feedback from customers and implementing customer management tactics. - Following Novartis specifications for documentation and tracking clinical trial milestones for assigned projects. - Maintaining records for all projects, including archiving and ensuring audit, SOP, and training compliance. - Training new team members and colleagues when required, in addition to performing any other assigned tasks. The minimum requirements for this role are: - Science degree or equivalent, B.Sc./equivalent with 8 years of Clinical Research (CR) experience, or M.Sc./M.Pharm +6 years of clinical research (CR) experience. - Desired qualifications include a Doctoral Degree or a Qualification in Medical Sciences (MBBS/MD/equivalent). - Alternatively, a PhD + 4 years of CR experience, MBBS/equivalent + 4 years of CR experience, or MD + 2 years of CR experience. Novartis is dedicated to reimagining medicine to improve and extend people's lives. By becoming a part of Novartis, you will contribute to our vision of becoming the most valued and trusted medicines company globally. If you are ready to join a mission-driven organization with a commitment to diversity and inclusion, consider applying to be a Medical Writer at Novartis. To learn more about our company culture and career opportunities, visit: [Novartis People and Culture](https://www.novartis.com/about/strategy/people-and-culture). Explore our benefits and rewards in the Novartis Life Handbook: [Novartis Benefits and Rewards](https://www.novartis.com/careers/benefits-rewards). Join the Novartis Network to stay connected and receive updates on future career opportunities: [Novartis Network](https://talentnetwork.novartis.com/network).

As a Scientific Sales Executive at JOGO Health Pvt Ltd, you will play a crucial role in driving sales for innovative EMG biofeedback products within hospital and healthcare settings. Your responsibilities will include: - Networking: You will be effective at building and maintaining relationships within the healthcare industry to foster trust and open new business opportunities. - Team collaboration: You should be willing to work cooperatively with cross-functional teams, including clinical and research units, for comprehensive client solutions. - Presentation skills: You are expected to have experience or aptitude in delivering product and research presentations to medical professionals and institutional clients. - Generate and qualify sales leads by identifying decision makers and key influencers in hospitals and healthcare institutions. - Present, promote, and sell JOGO's digital health solutions to existing and prospective customers using solid sales arguments and scientific product knowledge. - Build, develop, and maintain positive business and customer relationships to drive customer loyalty and revenue growth. - Collaborate with marketing, research, and clinical teams to organize scientific presentations and demonstrations for clients. - Participate in continuous training to maintain up-to-date product expertise and knowledge of digital healthcare advancements. - Support the company's mission by upholding the highest standards in ethics, compliance, and professional conduct. The company, JOGO Health Pvt Ltd, is a US-based multinational digital healthcare organization specializing in EMG biofeedback with a strong presence in India, the USA, Canada, and Malaysia. JOGO is globally recognized and holds the world's first JCI accreditation for a digital clinic. Required Qualifications: - B.Pharm - B.Sc - B.Tech - B.E,

You will be responsible for providing scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs). Additionally, you will provide medical and scientific input and information for business strategy for the region. Key Responsibilities: - Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs). - Plan, facilitate, and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product-specific campaigns. - Deliver scientific presentations with consistent messages for key products at various meetings. - Support scientific presentations at medical education meetings. - Understand and support Scientific Engagement (SE) activities as per Medical Plans. - Become an expert in oncology for GSK brands and associated activities. - Stay updated on scientific knowledge in oncology, GSK molecules, and their PI for effective on-label communications. - Support in the feasibility assessment of potential research sites, develop concept notes, proposals, budgets, and monitoring tools for field studies. - Provide medical inputs into the development and execution of brand strategy. - Support Named Safety contact in strengthening oncology Pharmacovigilance. - Ensure continuous self-learning in Pharmacovigilance. Qualifications Required: - Minimum Level of Education: MBBS with post-graduate qualification. - Preferred Level of Education: Post-graduate qualification in Pharmacology/Public Health. - Preferred Education Level Reason: To interact effectively with specialized HCPs. Job-Related Experience: - Excellent written and oral communication skills in English and the local language. - Experience presenting scientific topics in various settings. - Solid understanding of ICH-GCP principles and internal SOPs. - Ability to comprehend scientific methods and experimental design. - 1-2 years in the pharmaceutical industry, preferably in oncology therapy with a preference for Hemato-oncology. Other Job-Related Skills/Background: - Presentation skills at scientific meetings. - Effective communication skills, both verbal and written. - Technical writing skills. - Ability to stay updated with new developments. - Capacity to provide and receive constructive feedback. - Build and maintain relationships with colleagues. - Share knowledge with team members. - Collaborate effectively within a team to achieve common goals. - Contribute creative ideas for continuous improvement. - Develop strong relationships with key opinion leaders. --- **About the Company:** GSK is a global biopharma company focused on uniting science, technology, and talent to get ahead of disease together. Their purpose is to positively impact the health of 2.5 billion people by the end of the decade. GSK aims to prevent and treat diseases with innovation in specialty medicines and vaccines across therapeutic areas such as respiratory, immunology, inflammation, oncology, HIV, and infectious diseases. The company values creating an environment where employees can thrive and focus on delivering for patients, shareholders, and the community. **Inclusion at GSK:** As an inclusive employer, GSK encourages candidates to reach out if they require any adjustments during the recruitment process. Candidates can contact the Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss their needs. --- **Note:** GSK does not accept referrals from employment businesses/agencies without prior written authorization. If you receive unsolicited emails from email addresses not ending in gsk.com or job advertisements with suspicious instructions, please inform GSK at askus@gsk.com to verify the job's authenticity.,

As a Scientific Officer at the American Board of Education (ABE) in Kochi, Kerala, India, your primary role will involve coordinating and overseeing scientific research projects, supporting curriculum development, and providing guidance in related disciplines. You will be responsible for conducting and publishing research, advising on academic initiatives, and collaborating with educational institutions to enhance teaching strategies and student outcomes. **Key Responsibilities:** - Coordinate and oversee scientific research projects - Support curriculum development efforts - Provide guidance in related disciplines - Conduct and publish research in scientific fields - Advise on academic initiatives - Collaborate with educational institutions to enhance teaching strategies and student outcomes **Qualifications Required:** - PhD in any discipline - Outstanding English communication skills for writing, editing, and presentations - Strong analytical, organizational, and time-management skills - Proficiency with research tools, referencing styles, and MS/Google productivity suites - Experience in curriculum development is a plus - Experience in University Teaching and Research is a plus The American Board of Education (ABE) is a U.S.-based non-profit organization committed to accrediting post-secondary institutions and career colleges globally. Headquartered in Los Angeles, California, ABE evaluates academic quality, instructional delivery, and student outcomes, while supporting partner institutions in curriculum development and standardized program delivery. ABE certifies individual competencies through rigorous examinations and awards globally recognized professional credentials. In addition to accreditation, ABE provides strategic advisory services to enhance institutional performance and academic innovation. ABE's flagship School Research Program nurtures early talent, guiding students from grade eight to develop research skills and publish in international journals. To apply for this position, please email your resume (and a brief cover note) to careers@educationboard.us with the subject line "Scientific Officer - Kochi". Preferred Start Date: ASAP Compensation: Competitive; commensurate with experience EEO: The American Board of Education (ABE) is an equal opportunity employer.,

As part of Amgen's mission to serve patients living with serious illnesses, you will play a vital role in analyzing scientific requirements from Global Research and translating them into efficient information systems solutions. Your responsibilities will include: - Collaborating with cross-functional teams to identify data product enhancement opportunities - Performing data analysis, troubleshooting issues, and supporting system implementation and maintenance - Developing data product launch and user adoption strategy for Amgen Research Foundational Data Systems - Contributing your expertise in business process analysis and technology to drive operational efficiency and meet business objectives To excel in this role, you must have expertise in biopharma scientific domains and informatics solution delivery. You will collaborate extensively with global teams to ensure seamless integration and operational excellence. The ideal candidate will possess a solid background in the end-to-end software development lifecycle, be a Scaled Agile practitioner, and have experience in change management and transformation. Qualifications Required: - Masters degree with 1 to 3 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR - Bachelors degree with 3 to 5 years of relevant experience OR - Diploma with 7 to 9 years of relevant experience Basic Qualifications: - 3+ years of experience in implementing and supporting biopharma scientific research data analytics - Strong problem-solving skills and a passion for tackling complex challenges in drug discovery with data - Collaborative spirit and effective communication skills to work seamlessly in a multi-functional team - Commitment to continuous learning and staying updated with AI/ML advancements Preferred Qualifications: - Demonstrated expertise in a scientific domain area and related technology needs - Understanding of semantics and FAIR data concepts - Experience with cloud and on-premise compute infrastructure - Proficiency in creating impactful slide decks and communicating data effectively - Ability to deliver features meeting research user demands using Agile methodology Soft Skills: - Strong transformation and change management experience - Exceptional collaboration and communication skills - High degree of initiative and self-motivation - Ability to manage multiple priorities successfully - Team-oriented with a focus on achieving team goals - Strong presentation and public speaking skills Amgen is committed to providing a diverse and inclusive work environment, ensuring equal opportunities for all individuals. If you require any accommodations during the application process or employment, please contact us.,

As a Business Officer at Zuventus Healthcare Ltd. in Hyderabad, Telangana, your role will involve the following: - Communicating effectively with clients and stakeholders - Delivering engaging presentations - Utilizing your scientific background to understand and communicate product information - Influencing potential customers - Demonstrating strong selling skills - Having a strong orientation towards achieving targets To qualify for this position, you must have: - Graduated with a B.Sc or Bachelor of Pharmacy (B.Pharm) degree - Possess a Diploma in Pharmacy Please note that this role is based in the Odenea department of Zuventus Healthcare Ltd. within the ZHL Field vertical.,

As a Medical Scientific Expert at GSK, your main role will be to provide scientific and technical expertise for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs. You will also be responsible for providing medical and scientific input for business strategy in the region. **Key Responsibilities:** - Develop and maintain networking with Health Care Practitioners (HCPs). - Plan, facilitate, and conduct various scientific events and campaigns. - Deliver scientific presentations with consistent messages for key products. - Support and present at medical education meetings. - Understand and support Scientific Engagement activities. - Become an expert in oncology for GSK brands. - Stay updated on scientific knowledge related to oncology and GSK molecules. - Support in feasibility assessment of research sites and development of proposals. - Provide medical inputs for brand strategy. - Support oncology Pharmacovigilance efforts. **Qualifications Required:** - Minimum MBBS with post-graduate qualification. - Preferred post-graduate qualification in Pharmacology/Public Health. - Experience in presenting scientific topics and understanding ICH-GCP principles. - 1-2 years of experience in the pharmaceutical industry, preferably in oncology. At GSK, we aim to positively impact the health of 2.5 billion people by the end of the decade. We focus on specialty medicines and vaccines in therapeutic areas such as respiratory, immunology, oncology, HIV, and infectious diseases. Our culture emphasizes being ambitious for patients, accountable for impact, and doing the right thing. Join us in uniting science, technology, and talent to get ahead of disease together. Inclusion is a core value at GSK, and we encourage candidates to reach out for any necessary adjustments during the recruitment process. If you need any accommodations, please contact our Recruitment Team at IN.recruitment-adjustments@gsk.com. Please note that GSK does not accept referrals from employment businesses/agencies without prior authorization. Any unsolicited email or job advertisement not from an address ending in gsk.com should be disregarded. Kindly inform us at askus@gsk.com if you encounter any suspicious emails.,

Role Overview: As a Scientific Writer at the company, you will be responsible for providing high-quality writing support and project management of scientific communication projects in compliance with good publication practices. Your role will involve translating complex clinical data into clear and accessible content tailored to healthcare professionals (HCPs), patients, and other stakeholders both external and internal. Key Responsibilities: - Possess the ability to understand a therapeutic area and product strategy to ensure scientific communication objectives are met. - Learn quickly to understand a new therapeutic area and adapt work across multiple therapeutic areas. - Translate complex scientific information and clinical trial data into content that meets the needs of various audiences, including HCPs and patients. - Write key scientific communication deliverables such as abstracts, posters/presentations, and manuscripts. - Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure global content is relevant, up-to-date, and aligned with evolving data. - Maintain robust version control and document tracking to ensure transparency, audit-readiness, and traceability in Teva's publication tracking tool. - Establish relationships with authors, external experts, and clinical trial investigators to ensure efficient development of high-quality publications. - Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams to gain input and approval of scientific communication deliverables. - Follow Good Publication Practices and internal SOPs to ensure consistency and compliance. - Conduct peer reviews of content developed by other writers to uphold high-quality standards. - Participate in initiatives to enhance the content development process, including the use of AI tools, structured content libraries, and digital asset management systems. - Support the development of derivative content assets such as field medical affairs materials, congress preparation content, and other digital assets. Qualifications Required: - Education: Advanced degree (PharmD, PhD, MD, or Masters in Life Sciences or related field) required. - Language: English (Professional level competency) - Experience: 10-12 years of experience in medical writing, medical information, or scientific communications within the pharmaceutical, biotech, or medical device industry. - Experience with medical publication writing, scientific literature analysis, and congress content preparation. - Knowledge of Good Publication Practices and ICMJE Guidelines. - Familiarity with publication management systems (e.g., Datavision, Pubstrat, Komodo) and publication workflows. Role Overview: As a Scientific Writer at the company, you will be responsible for providing high-quality writing support and project management of scientific communication projects in compliance with good publication practices. Your role will involve translating complex clinical data into clear and accessible content tailored to healthcare professionals (HCPs), patients, and other stakeholders both external and internal. Key Responsibilities: - Possess the ability to understand a therapeutic area and product strategy to ensure scientific communication objectives are met. - Learn quickly to understand a new therapeutic area and adapt work across multiple therapeutic areas. - Translate complex scientific information and clinical trial data into content that meets the needs of various audiences, including HCPs and patients. - Write key scientific communication deliverables such as abstracts, posters/presentations, and manuscripts. - Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure global content is relevant, up-to-date, and aligned with evolving data. - Maintain robust version control and document tracking to ensure transparency, audit-readiness, and traceability in Teva's publication tracking tool. - Establish relationships with authors, external experts, and clinical trial investigators to ensure efficient development of high-quality publications. - Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams to gain input and approval of scientific communication deliverables. - Follow Good Publication Practices and internal SOPs to ensure consistency and compliance. - Conduct peer reviews of content developed by other writers to uphold high-quality standards. - Participate in initiatives to enhance the content development process, including the use of AI tools, structured content libraries, and digital asset management systems. - Support the development of derivative content assets such as field medical affairs materials, congress preparation content, and other digital assets. Qualifications Required: - Education: Advanced degree (PharmD, PhD, MD, or Masters in Life Sciences or related field) required. - Language: English (Professional level competency) - Experience:

As a Director, Business Development at Red Nucleus, your main responsibility is to develop and execute strategic account growth plans across both new and existing accounts. You will work with the Scientific Services & Advisory (SS&A) team to sell and position solutions to key decision-makers within R&D, Commercial, and IT sectors. Your role will involve opening doors to new accounts, expanding existing accounts, creating strategic account development plans, developing client relationships, setting up meetings with key stakeholders, and ensuring profitability targets are met. Additionally, you will collaborate with internal teams to craft appropriate solutions for identified opportunities. - Open doors to new accounts for business and technology consulting services - Expand accounts once opened (new and existing) - Align with SS&A partners to ensure sales strategy meets Business Unit vision - Create and update Strategic Account Development Plans - Develop strong client relationships within target accounts and external partners - Set up meetings with key decision-makers to identify, qualify, consult, and close opportunities - Collaborate with internal service delivery teams to craft appropriate solutions - Write proposals, develop presentations, and draft SOWs - Manage and track pipeline and opportunities - Ensure all business sold meets profitability targets - Provide input towards targeted Marketing initiatives Qualifications Required: - Proven success in achieving, maintaining, or exceeding $3M-5M sales target annually - Solid network across Life Sciences for consulting services - Experience in selling business and technology consulting services - Ability to break into new accounts and functional areas within existing accounts - Demonstrated ability to develop and grow client relationships across functional areas - Excellent written and verbal communication skills - Strong collaboration skills within cross-functional teams - Understanding of the pharma sector with a focus on consulting services - Prior experience with SalesForce as a CRM tool desired - Advanced skill level in MS Excel, Word, PowerPoint, and Outlook - Understanding of the drug development process - Up to 50% travel required,

Role Overview: As a Medical Advisor at Intas Pharmaceuticals, you will be responsible for handling the medico marketing responsibilities of the assigned business unit/s. Your role will involve strategic support, customer engagement, and training and development in the medical and scientific aspect of the business. Key Responsibilities: - Strategic Support: - Serve as an internal medical and scientific resource to assigned therapeutic areas - Support in devising Product/Therapy Strategy - Provide medical/clinical oversight regarding positioning strategy and implementation tactics for respective products - Stay updated on new developments, publications, and trends in different therapy areas - Work closely with Business Development to identify new molecules and novel drug delivery systems in alignment with business needs - Customer Engagement: - Identify, develop, maintain, and leverage professional relationships with national KOLs and key customers - Interact with HCPs to answer scientific, product, and therapy-related questions - Deliver scientific presentations and medical education to healthcare professionals - Conduct and coordinate various scientific initiatives like CMEs, RTMs, and symposia - Training and Development: - Provide training on therapy/product updates for therapy management and Training and Development team - Contribute to the knowledge upgradation initiatives/activities on therapy/molecules for the Field Force team Qualification Required: - Medical graduate/Postgraduate (MBBS/MD/MS) + Management qualification - 2-3 years of medico marketing experience with team handling At Intas Pharmaceuticals, success is attributed to the strength of its people. The company is committed to attracting and retaining the best talent in the industry while fostering an environment that encourages innovation and excellence. By joining Intas, you will play a meaningful role in driving both the company's growth and advancements in global healthcare.,

Role Overview: You will be responsible for preparing consistent and high-quality technical documents related to Pharmaceutical Research and Development for Formulation at Teva. Your role will involve executing all functions in accordance with current FDA regulations, ICH guidelines, USP methodologies, cGMPs, and SOPs. Maintaining open communication with R&D members to ensure timely delivery of high-quality documents independently with minimal supervision will be a key aspect of your responsibilities. Key Responsibilities: - Prepare documents and facilitate documentation management in R&D while ensuring correctness, completeness, and clarity following established guidelines. - Prepare documents such as Manufacturing Batch Records, Study Protocol and Reports, Stability Protocols, Product Development Report, Quality Overall Summary, response to regulatory queries based on scientific input from the Formulation team. Knowledge of QBD & DOE is essential. - Prepare high-impact presentations including graphs and charts. - Submit documents for signatures, coordinate their flow, archival, and retrieval to ensure timely flow and publish monthly performance metrics. - Continuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements. - Perform other duties as assigned or delegated. - Comply with FDA guidelines/Company Policies of Data Integrity. Qualifications Required: - Education: A minimum of a master's degree (M.Pharm) or a PhD in Pharmacy is required. - Industry Experience: Minimum 12 to 15 years of Formulation R&D experience with solid oral dosage forms for regulated markets. Knowledge of other dosage forms will be an added advantage. - Demonstrated knowledge and understanding of quality and regulatory guidance for SOD products for regulated markets. - Demonstrated knowledge and working understanding of basic concepts of Good Manufacturing Practices (GMP), regulatory documentation required. Additional Company Details: Together, Teva is on a mission to make good health more affordable and accessible worldwide. As the world's leading manufacturer of generic medicines, Teva is dedicated to helping millions enjoy healthier lives. With a presence in nearly 60 countries and a diverse workforce, Teva is always looking for new ways to make a difference and welcomes individuals who share the same mission. Note: The job description did not include any additional details about the company.,

In this role, you will report to the Regional Medical Director and function as the affiliate's medical/scientific expert for assigned product(s) and relevant therapeutic areas in the South Asia region. Your duties will involve offering medical and scientific guidance to key customers, contributing to marketing strategy, supporting clinical research projects, and ensuring compliance with regulations and company policies. Additionally, you will be a part of the ADC local leadership team. Your key responsibilities will include: - Developing and maintaining in-depth knowledge of assigned product(s) and diabetes care through internal meetings, congresses, seminars, and literature review - Providing expert medical/scientific advice, responding to requests for information, and contributing to the development of core dossiers - Establishing and maintaining relationships with key opinion leaders and academic centers through scientific congresses, advisory boards, and meetings - Delivering scientific presentations and education programs to healthcare professionals - Screening relevant literature and scientific information for key messages, and providing training to sales forces and other departments - Supporting clinical research projects, managing local Investigator Initiated Studies, and reviewing promotional material for compliance - Monitoring competitive intelligence, providing input into marketing strategy, and ensuring regulatory compliance - Effectively utilizing resources, planning and delegating tasks, analyzing and problem-solving, and operating within budget - Maintaining up-to-date scientific knowledge, supporting sales/marketing teams, and communicating effectively with internal and external clients - Demonstrating good judgment on compliance issues, practicing effective communication and negotiation skills, and prioritizing activities for organizational goals Qualifications required for this role are: - Minimum 6 years of experience in the pharmaceutical/medical device industry - General knowledge of drug development and clinical research is an advantage - Keen interest in developing and maintaining expert knowledge in the assigned therapeutic area/product - Excellent verbal and written communication skills, including strong presentation abilities - High customer orientation and stakeholder relationship skills - Commitment to compliance, scientific quality, and integrity - Good understanding of written English - Willingness to travel at least 30-40%,

As a Research Analyst (Scientific Writing) at our company, you will play a crucial role in supporting the development of high-quality scientific documents, publications, and research-based content. Your strong background in life sciences, biotechnology, or pharmaceuticals, combined with excellent skills in scientific writing, data interpretation, and literature analysis will be key in transforming complex scientific data into clear, accurate, and impactful content for various deliverables. **Responsibilities:** - Conduct in-depth literature reviews and gather relevant scientific data from peer-reviewed journals, databases, and clinical reports. - Analyze and synthesize scientific information to prepare well-structured documents, including research summaries, manuscripts, white papers, and regulatory content. - Collaborate with scientists, subject matter experts, and cross-functional teams to ensure accuracy, clarity, and consistency of written materials. - Prepare data-driven reports and presentations for internal and external stakeholders. - Ensure compliance with scientific, ethical, and regulatory writing standards (e.g., ICH, GCP, CONSORT, or similar). - Stay updated with current developments in life sciences, healthcare, and biotechnology sectors. **Requirements:** - Master's or PhD in Life Sciences, Biotechnology, Pharmacy, Medicine, or related field. - Proven experience in scientific/medical writing or research analysis. - Strong ability to critically analyze data and translate complex concepts into clear, concise narratives. - Proficiency with scientific databases (PubMed, Embase, Scopus, etc.) and reference management tools (EndNote, Mendeley, Zotero). - Excellent written and verbal communication skills with attention to detail. - Familiarity with statistical analysis and clinical trial design is a plus. - Ability to work independently, manage deadlines, and handle multiple projects. In addition to the exciting responsibilities and requirements, we offer you: - Opportunity to work on impactful projects in the life sciences and healthcare sector. - A collaborative environment with scientists, researchers, and industry experts. - Professional development and training in scientific writing and research methodology. - Competitive compensation package with growth opportunities.,

As a Research Publication Writer, your primary responsibility will be to produce high-quality, original manuscripts and other scholarly articles for submission to reputable, peer-reviewed journals. You will collaborate closely with researchers, subject matter experts, and editors to ensure the clear, concise, and ethical presentation of complex scientific information. Key Responsibilities: - Manuscript Drafting: Draft, structure, and organize research papers, review articles, white papers, and other documents from initial data and researcher input. - Research & Analysis: Conduct thorough literature reviews and editorial research to ensure content accuracy, relevance, and a comprehensive understanding of the subject matter. - Editing & Proofreading: Edit and proofread all materials to ensure impeccable grammar, clarity, consistency, and adherence to specific journal guidelines and style manuals (e.g., APA, AMA, Chicago). - Data Presentation: Work with researchers to present complex data, figures, and results in a clear, logical, and visually appealing manner. - Compliance & Ethics: Ensure all publications adhere to ethical standards, including proper citation, data integrity, originality, and the handling of conflicts of interest. - Collaboration: Liaise with internal and external stakeholders, including co-authors, editors, and publishers, to manage the submission and peer-review process, and implement revisions based on feedback. - Project Management: Manage multiple writing projects simultaneously, prioritize tasks effectively, and consistently meet tight publication deadlines. - Vendor Management and clinical outsourcing for ongoing and upcoming projects in CDMA department Qualifications Required: - Education: A Bachelor's or Master's degree in a relevant field (e.g., Physical Sciences, Life Sciences, Engineering, English, Journalism, or Communications). A PhD is highly advantageous. - Experience: Proven experience (e.g., 2+ years) in academic or scientific writing and editing, with a strong portfolio of published work. Experience within a peer-reviewed journal publisher or a similar research environment is a plus. - Writing Skills: Exceptional writing, editing, and verbal communication skills, with the ability to distill complex information into clear and compelling content for a specific audience. - Research Skills: Strong research and analytical abilities, with experience in navigating academic databases (e.g., Google Scholar, PubMed). - Technical Proficiency: Familiarity with manuscript submission systems, content management systems, and reference management software. Proficiency in Microsoft Office Suite is essential. - Soft Skills: High attention to detail, strong organizational and project management skills, critical thinking, and the ability to work both independently and collaboratively in a team environment.,

As a Medical Affairs Specialist, you will play a pivotal role in supporting the marketing and sales teams with scientific expertise. You will collaborate across functions to ensure the accuracy and scientific integrity of marketing materials, product launches, and ongoing brand management. This role requires a deep understanding of scientific data and the ability to communicate it effectively to non-scientific stakeholders. - Conduct comprehensive literature reviews to support the creation of medical manuals, presentations, and marketing materials. - Lead the development of product launch presentations, delivering insights on therapy areas and product specifics to the marketing and sales teams. - Serve as the scientific point of contact for the field force and healthcare professionals, providing accurate, evidence-based responses to support relationships with customers. - Stay up-to-date with scientific data, clinical trials, and guidelines relevant to the company's products and therapy areas. - Provide technical support to marketing and sales teams, ensuring scientific accuracy in all materials. - Develop and deliver training programs (fresher and refresher) for medical representatives, ensuring they are well-versed in the latest product and therapeutic information. - Provide medical insights and rationale for new product development, including product ideation and evaluation for new indications and dosage forms. - Prepare and contribute to manuscripts for peer-reviewed journals, focusing on original research and review articles related to the company's products and therapeutic areas. Qualifications: - Educational Requirement: M. Pharma or equivalent degree in a relevant field. - Experience: Minimum 1-3 years in a similar role, preferably within the pharmaceutical or healthcare industry. Skills & Competencies: - Strong understanding of scientific concepts in pharmaceutical products and therapy areas. - Ability to simplify complex scientific information for non-scientific stakeholders. - Proficiency in scientific content creation, medical writing, and presentation development. - Knowledge of regulatory guidelines and industry standards related to medical marketing and publications. - Excellent communication, presentation, and interpersonal skills. - Ability to thrive in a cross-functional, fast-paced environment. In addition, the job offers competitive salary, career growth opportunities in a leading pharmaceutical organization, and exposure to a broad range of therapeutic areas and product lines. The benefits include health insurance, life insurance, and provident fund. Please note that the work location is in person at Mumbai, Maharashtra.,

As a Sr. Sales Engineer for CAD/CAM Solutions and 3D Printing in Pune, with 2-6 years of experience, your role involves promoting and selling cutting-edge products like Dassault Systmes Discovery Studio, Bio 3D printers, Stratasys 3D printers, and Artec 3D scanners. Your primary focus will be on revenue generation through identifying and pursuing sales opportunities within the designated market segment. **Key Responsibilities:** - **Product Knowledge:** Develop a comprehensive understanding of the features, functionalities, and applications of the products. Stay updated on the latest advancements in the field. - **Sales Strategy:** Identify and target potential customers from research institutions, educational organizations, biotechnology companies, and other relevant industries. Develop and execute effective sales strategies to achieve targets. - **Customer Engagement:** Build relationships with key stakeholders, understand their needs, provide product demonstrations, and tailor solutions to address customer requirements. - **Lead Generation:** Proactively identify and generate leads through various channels and convert them into sales opportunities. - **Proposal Development:** Prepare compelling proposals and presentations for prospective clients, collaborating with internal teams to develop customized solutions. - **Sales Negotiation and Closing:** Lead negotiations, address objections, and close sales deals within defined timelines while ensuring customer satisfaction. - **Market Analysis:** Conduct market research to identify trends, competitor activities, and provide feedback to the management team. - **Collaboration:** Work closely with sales, marketing, and technical support teams to ensure effective customer support throughout the sales cycle. **Qualifications:** - **Bachelors Degree:** in engineering, science, or related field. - **Sales Experience:** Proven track record in sales, preferably in scientific, biotechnology, or 3D printing industry. - **Technical Aptitude:** Strong understanding of the products. - **Communication Skills:** Excellent communication and presentation skills to convey technical concepts effectively. - **Relationship Building:** Demonstrated ability to build and maintain customer relationships. - **Self-Motivated:** Target-driven and able to work independently. - **Willingness to Travel:** Travel as needed to meet clients, attend events, and represent the company.,

As a Scientific Affairs Manager at MedGenome Labs Ltd in New Delhi, you will play a crucial role in the clinical genomic space by leveraging your specialized product knowledge to support doctors and clinicians. Your responsibilities will include: - Utilizing your 3+ years of experience in Diagnostics to focus on specialized products targeted at doctors/clinicians - Demonstrating expertise in Clinical Reporting with a specific emphasis on Oncology/Reproductive genomics - Organizing CMEs/doctor group meetings in collaboration with sales teams to address company priorities - Engaging in fieldwork with sales teams to establish relationships with Key Opinion Leaders (KOLs) and gather feedback to enhance scientific services and brand perception - Showcasing excellent communication and presentation skills to effectively convey scientific information - Travelling within the north region to meet doctors and clinicians for collaborative opportunities To qualify for this role, you should possess a Ph.D. or Masters in Human Genetics, Life Science, or related studies. MedGenome Labs Ltd is a market leader in the clinical genomic space in India, operating the largest CAP accredited Next Generation Sequencing (NGS) lab in Southeast Asia. As a founding member of GenomeAsia 100K, an initiative to sequence 100,000 Genomes in Asia, the company is at the forefront of genomic research and diagnostics. If you are passionate about advancing genomic research and have the requisite experience and qualifications, we encourage you to apply for this exciting opportunity.,

As a Senior Content Manager at Centrix Healthcare, a leading medical communications company in Mumbai, your role involves leading the development of high-quality scientific content across various formats to support medical symposia, doctor upskilling courses, speaker programs, and academic initiatives. You will collaborate with internal teams, pharma clients, and medical experts to ensure that the content is clinically accurate, engaging, and strategically aligned. Your key responsibilities will include: - Designing program brochures, newsletters, and invitations for HCP-targeted campaigns. - Developing content modules for doctor upskilling courses (CME/e-learning). - Creating agendas for symposia and webinars in collaboration with pharma teams. - Drafting key takeaways, post-event summaries, and speaker scripts. - Supporting international speakers in presentation development and slide storytelling. - Preparing questionnaires for KOL interviews and advisory board summaries. - Rewriting abstracts/posters and compiling conference highlight reports. - Assisting doctors in paper writing, presentations, and literature reviews for academic purposes. - Coordinating with internal design/digital teams to package content in engaging formats. - Ensuring content aligns with clinical evidence, brand strategy, and regulatory norms. Qualifications required for this role include: - Degree in Pharmacy, Medicine, or Life Sciences (e.g., MPharm, MBBS, MD, MSc). - 7-10 years of experience in medical writing or scientific content in a healthcare or pharma support role. - Strong understanding of clinical data, therapy guidelines, and pharma communication formats. - Excellent writing, summarizing, and content structuring skills. - Ability to work effectively with doctors, pharma clients, and design teams in a fast-paced environment. As a full-time permanent employee at Centrix Healthcare, you will be entitled to benefits such as food, Provident Fund, performance bonuses, and yearly bonuses. The work schedule involves day shifts with a fixed morning schedule at the onsite work location in Mumbai. If you are passionate about scientific communication and possess the required qualifications and experience, we encourage you to apply for this exciting opportunity by reaching out to hrc@centrixhealthcare.com.,

You are seeking a motivated and creative Scientific Communication Intern to join the dynamic team at sftwtrs.ai, a leading AI/ML research laboratory. This internship offers a unique opportunity to bridge the gap between complex scientific concepts and public understanding. Key Responsibilities: - Create engaging content for various digital platforms to communicate research findings and technological innovations - Develop and maintain social media presence across multiple platforms - Collaborate with researchers to translate technical concepts into accessible content - Assist in creating visual content and infographics to explain complex AI/ML concepts - Support the development of presentation materials and research summaries Qualifications Required: - Currently pursuing a degree in Communications, Journalism, Scientific Writing, or a related field - Strong written and verbal communication skills - Proficiency in social media management tools - Basic understanding of AI/ML concepts - Ability to work independently and as part of a team Preferred qualifications include: - Experience with graphic design tools (Adobe Creative Suite, Canva, etc.) - Knowledge of data visualization techniques - Previous experience in science communication or technical writing - Understanding of digital marketing principles sftwtrs.ai offers hands-on experience in a cutting-edge AI research environment, mentorship from experienced professionals, an opportunity to build a professional portfolio, and flexible working hours. sftwtrs.ai is an Equal Opportunity Employer, actively encouraging applications from candidates of all genders, backgrounds, and experiences. The commitment to diversity and inclusion is reflected in hiring practices and workplace culture. Duration: 3-6 months Location: On-site Compensation: Competitive stipend provided To apply, please submit your resume, portfolio (if available), and a brief cover letter explaining your interest in science communication and AI/ML technology. Job Type: Full-time Schedule: Monday to Friday Experience: Total work: 1 year (Preferred) Work Location: In person,

As a Hematology Territory Account Manager for a leading biotech organization focused on developing transformative gene therapies for Sickle Cell Disease (SCD) and Transfusion-Dependent -Thalassemia (TDT) in the Midwest region, your role will be crucial in accelerating patient access and adoption of breakthrough therapies. You will play a key role in building awareness, driving referrals, and supporting healthcare providers across Illinois, Michigan, Minnesota, Ohio, and Wisconsin. Key Responsibilities: - Serve as the primary point of contact for referring physicians, community clinics, and treatment centers, offering guidance on patient identification, referral pathways, and therapy administration. - Educate healthcare teams on the clinical profile, patient journey, and treatment considerations for SCD and TDT, effectively translating complex scientific data into actionable insights. - Develop and execute a territory strategy that emphasizes community outreach and treatment-center alignment, ensuring consistent engagement across affiliated and unaffiliated accounts. - Utilize data and insights to identify high-value physician targets, optimize engagement, and monitor progress towards adoption and access goals. - Collaborate with internal cross-functional teams to streamline patient access, overcome barriers, and coordinate account-level efforts. - Maintain a deep clinical expertise in hematology, including SCD, TDT, and Hematopoietic Stem Cell Transplantation (HSCT), to facilitate credible, science-driven discussions. - Attend key conferences and professional meetings to build relationships, share insights, and contribute to strategic initiatives. - Effectively use digital tools and CRM systems to document interactions, track performance, and support strategic decision-making. - Operate ethically, compliantly, and professionally while managing a large, dynamic territory. Qualifications: Experience & Background: - Bachelor's degree required - 5+ years of experience in pharmaceutical or biotech sales, preferably in rare disease, hematology, cell/gene therapy, or related specialty products - Demonstrated ability to launch or manage complex therapies in hospital, specialty, or multi-site care settings - Familiarity with infused biologics, hospital operations, and therapy distribution models - Strong understanding of clinical workflows and provider decision-making in hematology and rare disease - Comfortable navigating community and referral networks, influencing without formal authority Skills & Attributes: - Exceptional communication skills, capable of presenting scientific data clearly to both technical and non-technical audiences - Strategic thinker with the ability to translate insights into actionable account plans - Highly self-motivated, resilient, and able to manage a large, dispersed territory with 50-100% travel - Collaborative team player with emotional intelligence, capable of effective cross-functional partnerships - Proficient in leveraging digital tools for customer engagement and data-driven decision-making By taking on this role, you will play a vital part in overcoming the challenges faced by patients with SCD and TDT in accessing innovative therapies. Your efforts will be instrumental in connecting physicians and treatment centers to life-changing therapies, ultimately driving measurable patient impact across a complex and high-stakes landscape.,