8 Endnote Jobs

Company Overview: FIDELITY HEALTH SERVICES is a global pharmacovigilance company focused on patient safety and regulatory compliance. With offices in Toronto, London, Mumbai, Pune, and Ahmedabad, we deliver tech-driven safety and quality solutions to pharmaceutical and biopharmaceutical clients worldwide. Role Summary: Full-time, On-site Literature Search Specialist Medical Services (Mumbai) Responsible for conducting comprehensive literature searches across scientific databases (e.g., PubMed, Embase, Google Scholar) for drug safety and regulatory purposes. Perform systematic and targeted searches for aggregate reports, signal detection, and risk management activities. Screen and evaluate sc...

Please share below details to [HIDDEN TEXT] Candidate Name Mobile No. Email ID Current Company Exp. Notice Period Current Location Preferred Location CCTC ECTC Role Overview: The Medical device Literature Librarian identifies and retrieves published information on clinical safety and performance outcomes for medical devices. He/She supports systematic literature reviews, evidence-based research, and regulatory submissions by identifying, retrieving, and organizing scientific literature using advanced search strategies and bibliographic databases. The Medical device Literature Librarian should meet the following professional standards to ensure competence in executing regulatory literature su...

We are seeking a highly skilled Scientific Content Production Individual accountable for content creation of medical publications and communications. The ideal candidate will have proven expertise in Scientific Writing, planning and strategy in the pharmaceutical industry. Candidate will be closely working with peer writers and will be responsible for the training of the team. What will you Do Able to conduct literature searches (PubMed, EMBASE, clinicaltrial.gov, EudraCT, congresses, COCHRANE), screening, data extraction, and analysis to support content development. Independently compiles, writes, and edits medical writing deliverables including operating guidance documents, SOPs, training ...

Role Overview: As a Global Systematic Literature Review (SLR) Manager at Amgen's Global Health Economics & Outcomes Research (HEOR) department based in Hyderabad, India, your main responsibility will be to design, execute, and manage literature review services. You will work closely with Global HEOR Product Leads to ensure alignment with HEOR product strategy, ultimately supporting global access to Amgen's therapies through the generation of high-quality, evidence-based outputs. Key Responsibilities: - Refine literature review questions in collaboration with Global HEOR Product Lead and prepare research protocols. - Develop inclusion/exclusion criteria within the PICO framework. - Design lit...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll 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 busines...

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...

Roles & Responsibilities Ensure on-time development and delivery of various sections of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across therapeutic areas Actively engage with internal stakeholders and cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs Deliver solutions that are customized per client requirements in terms of language, content, format, and presentation Assist the Team Lead/Manager in the development of schedules to ensure timely delivery Manage timelines and communicate with team members to maintain awareness of expectations, m...

Roles & Responsibilities Ensure on-time development and delivery of various sections of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across therapeutic areas Actively engage with internal stakeholders and cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs Deliver solutions that are customized per client requirements in terms of language, content, format, and presentation Assist the Team Lead/Manager in the development of schedules to ensure timely delivery Manage timelines and communicate with team members to maintain awareness of expectations, m...