518 Scientific Writing Jobs - Page 15

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Medical Writer / Technical Content Writer - Internship This internship is ideal for someone passionate about simplifying medical or technical information into clear, structured documents and engaging content. Good Knowledge of Medical terminology. Required Candidate profile Preparation of protocol for Clinical trials Preparation writing CSR (Clinical Study Report) BDS and MBBS With medical writing for clinical trials Knowledge are Applicable

As a Medical Writer with our dynamic team, you will utilize your expertise in writing, editing, and reviewing scientific and medical content. Your primary responsibility will involve transforming intricate medical data and research findings into clear, accurate, and engaging documents suitable for various audiences, including healthcare professionals, regulatory bodies, and the general public. You will be expected to develop, write, and edit a diverse range of documents such as clinical study reports, regulatory submission documents, peer-reviewed publications, and educational materials. Your role will also involve generating high-quality manuscripts, abstracts, posters, and presentations fo...

Education - MD specialisation in Microbiology. Job Summary We are seeking a dedicated MD in Microbiology to join our Medical Affairs team. The role involves close collaboration with the Medical Affairs Head to support reporting, documentation, and data analysis related to clinical and scientific projects. The position is based in Navi Mumbai, with potential travel and meeting participation as part of the job. What We Want You To Do Assist the Medical Affairs Head in drafting, reviewing, and organizing scientific and clinical reports. Analyze clinical data and contribute to interpretation and presentation of findings. Coordinate internal communications and documentation flow within the Medica...

Scientific Lead - Medical Nutrition (MD) Are you a medical doctor with deep clinical expertise, a flair for scientific storytelling, and strong KOL relationships in Delhi NCR? What You will Do: Act as the scientific face of the organization for clinical nutrition solutions Engage meaningfully with key medical experts across critical care, internal medicine, respiratory medicine, and nutrition therapy Drive scientific education, knowledge sharing, and real-world clinical insights across the medical community Collaborate closely with commercial, marketing, and regulatory teams to align strategy and communication Lead initiatives to develop regionally relevant clinical evidence. What Were Looki...

Position Description: The Commercial Learning Services (CLS) Medical Writer is responsible for the development of medical content including but not limited to creating/ updating wireframes, building reference packages, creating/ updating learning content for product trainings for assigned areas at both Global and affiliate level. The CLS Medical Writer will anticipate and adjust for problems and roadblocks, interface with Lilly partners at Indianapolis and Lilly Bengaluru and integrate new business processes where necessary. Using strong adult learning principles, CLS Medical Writer ensures quality design, development, and delivery of training development projects. This role will interact wi...

Department New Generation Insulin (NGI) The Position As a Regional Medical Advisor, you will contribute actively to medico-marketing activities in the business area/portfolio and support in implementation of the Medical Affairs strategy in the country. You will be responsible for: Executing the Indian medical strategy into local activities in your designated region Building, maintaining, and nurturing the excellent scientific relationship with all the key influencers and stakeholders Training and educational activities for Physicians and other Health Care Professionals (HCPs) working with diabetes and obesity Medical support to brand team You will also be responsible for: To assist the marke...

Role & responsibilities As a Project Executive (Content Writer) at Cognus Technology, you will play a key role in crafting high-quality, well-researched academic content specifically in the Finance and Medical domains. Youll be responsible for understanding client requirements, conducting in-depth research, and delivering original, insightful content aligned with academic standards. This role is ideal for candidates with a passion for research, strong analytical thinking, and the ability to simplify complex concepts into clear, structured academic documents. Key Responsibilities: Research & Content Creation: Conduct comprehensive research on topics related to Finance and Medical domains. Cre...

As a member of our global team in the Data Sciences organization, you will play a crucial role in establishing scientific excellence in the development of digital biomarkers and endpoints. Your primary responsibility will be leading the identification, development, and deployment of novel digital endpoints and outcome measures across clinical trials and life cycle management programs. This will involve close collaboration with the Global Digital Health organization to design and validate algorithms extracting clinically relevant insights from various digital health data sources. Your expertise will ensure scientific rigor, clinical validity, and regulatory readiness in this process. In this ...

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and respond...

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessfu...

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessfu...

Job responsibilities include some of the following: Product & Process Knowledge Management: Data gathering ( Product Quality Review, Change Requests, Methods of Production, Genealogical tree and quality reporting, PHF Parking lot (document with the pending point of the previous version of PHF. Manage PHF governance & operational follow up meetings: (kick off, consolidation, follow up ) Write/update the PHF s with information gathered and manage the approval process with identified stakeholders. PHF Publishing in Veeva, Manage AAR with stakeholders, PHF continuous improvement Collaboration and Communication: Work collaboratively with various departments, including MSAT discipline experts, QA,...

Summary The Medical Expert in TCO (Translational Clinical Oncology) is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical co-leadership for assigned aspects of one or more global, active, TCO study, under the leadership of a Clinical Program Leader (CPL) TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for ...

JOB DESCRIPTION: JOB CODE: BIOPLUS/MEDCOMM/WH/020 DATE OF CREATION: 7th Feb 2025 Department Marketing/ Medico-marketing Communications Position Scientific Writer / Sr. Scientific Writer Reports to General Manager Marketing Communications Qualification Ph. D/ M. Pharm / B. Pharm / MBBS / BDS / MDS / BAMS / BHMS/ PG in life sciences. Experience Total 4 Years experience in Medico-Marketing in the Pharmaceutical Industry. 3+ years experience in developing scientific and medico-marketing content development for pharmaceutical companies Strong written and verbal communication/presentation skills Ability to translate complex medical concepts into easy-to-understand marketing messages. Ability to co...

Key Responsibilities: Lead team and oversee content delivery Develop scientific content Manage timelines and strategy Train team and ensure compliance Health insurance Maternity benefits in mediclaim policy Performance bonus Referral bonus Provident fund Paternity leaves Career break/sabbatical Prevention of sexual harrassment policy

A Day in the Life The Clinical Evaluation Medical Writer on our Endoscopy team plays a key role in developing and updating clinical evaluation documents (e.g., CEP, CER, PMCFP, PMCFR, SSCP) to support CE Mark submissions and maintain compliance throughout the product lifecycle. This work follows MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745 and involves close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk. In addition, the writer supports related activities such as summarizing and disseminating clinical literature and other available data to share relevant evidence, while also managing Medical Information activities. Th...

About the job: Key responsibilities: 1. Conduct research and experiments to develop innovative biotechnology solutions 2. Utilize scientific writing skills to prepare reports, presentations, and publications 3. Proficiency in MS-Word and MS-Excel to analyze data and document findings 4. Collaborate with cross-functional teams to ensure project milestones are met 5. Demonstrate effective communication skills to present findings to stakeholders 6. Apply knowledge of biology to drive product development and testing 7. Stay current on industry trends and advancements to contribute to continuous improvement efforts Who can apply: Only those candidates can apply who: Salary: ₹ 2,00,000 - 4,00,000 ...

The Content Solutions team at Indegene focuses on diverse projects throughout the product life cycle, covering regulatory, safety, medical affairs, and commercial solutions for clients. Leveraging clinical and scientific knowledge, the team addresses various business challenges to engage target audiences such as physicians and patients in different therapy areas. As a member of the team, you will have the opportunity to collaborate with healthcare clients on a variety of projects. Indegene is currently seeking a Scientific Writer and Reviewer to fulfill the role of a quality medical reviewer/technical reviewer for promotional, disease education, and training materials on behalf of a pharmace...

RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelli...

The Lv Prasad Eye Institute is renowned for its cutting-edge research and contributions to the field of ophthalmology. Focused on providing world-class eye care solutions, the institute aims to innovate and advance eye care through extensive research and development programs. It is a prominent center for learning and collaboration among eye care professionals. This full-time, on-site role located in Hyderabad is for a Research Optometrist. The responsibilities include conducting clinical research, collecting and analyzing data, and collaborating with other researchers and clinicians. Daily tasks encompass performing eye exams, conducting electrophysiology tests, contributing towards clinical...

As a member of our global team, you will play a crucial role in fostering scientific excellence in the field of digital biomarkers and endpoints within the Advanced Data Science team of the Data Sciences organization. Your primary responsibilities will include leading the identification, development, and implementation of innovative digital endpoints and outcome measures across various clinical trials and life cycle management programs. By collaborating closely with the Global Digital Health organization, you will be instrumental in designing and validating algorithms that extract clinically relevant insights from a diverse range of digital health data sources, such as wearables, sensors, an...

A Research Scientist designs, conducts, and analyzes experiments and research projects to advance scientific knowledge and potentially develop new products or technologies. They are responsible for all stages of research, from planning and execution to data analysis and reporting, and often collaborate with other scientists and professionals. Key Responsibilities: Planning and Design: Developing research proposals, designing experiments, and creating research plans. Execution: Conducting experiments, collecting data, and monitoring research progress. Analysis and Interpretation: Analyzing data, interpreting results, and drawing conclusions. Reporting: Writing research papers, reports, and pr...

The Medical-Regulatory Writer Assistant Manager will be responsible for planning and managing Medico-Regulatory Writing for Regulatory compliance in accordance with applicable Regulatory Guidelines. You will be tasked with providing high-quality medical and scientific writing services, from planning and coordinating literature searches to delivering final drafts to both internal and external clients. Your role will also involve offering technical consultation, substantive advice on strategy, regulations, and industry best practices, and demonstrating expertise in subject matter and therapeutic areas. In addition, you will need to effectively manage medical writing projects to ensure the deli...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here youll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing imp...