Medical Writing Associate

Company Description Jehangir Clinical Development Centre (JCDC) is a global, clinical-stage full-service CRO providing comprehensive support for Phase I-IV clinical trials, validation studies, real world evidence (RWE) studies, and biobanking projects. With over 350 successfully executed clinical projects, JCDC has a proven track record in developing...

We are hiring Pharma SME – Medical Writing Experience: 5–8 yearsIndustry: PharmaceuticalShift Timing: 2 pm to 11 pmLocations: Pune/Bangalore/LucknowKey Responsibilities:Develop, review, and finalize scientific and regulatory documents including clinical study reports (CSRs), protocols, investigator brochures (IBs), and safety narratives.Ensure all...

**Responsibilities**: **Years of Experience: 2 to 3 years relevant experience** **Role Description**: - Support sales goals by reviewing required information on a timely basis consistent with provided guidance - Support profitability goals by summarizing medical information accurately **Reporting relationship**: This role will report to Operations -...

Role DescriptionThis is a full-time on-site role for aMedical Device - Medical Writer (PMS)located in Pune. The Medical Writer will be responsible for creating scientific and medical content, conducting research, and writing medical communications. Day-to-day tasks include developing and editing documents related to post-market surveillance (PMS) and...

**Medical Writer Roles and Responsibility** - Creating, proofreading and editing regulatory and clinical documents, Investigator brochures. - Directly involved in medical marketing of new FDA drugs, pharmaceutical products, equipment through writeups, blogs, information handouts/leaflets, etc. - Coordination with physicians, scientists and healthcare...

Summary of Responsibilities:Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. (Language of communication: French)24x7 rotational shiftsReceive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs)...

Creating, proofreading and editing regulatory and clinical documents, Investigator brochures. - Directly involved in medical marketing of new FDA drugs, pharmaceutical products, equipment through writeups, blogs, information handouts/leaflets, etc. - Coordination with physicians, scientists and healthcare professionals for whereabouts of ongoing research and...

To write an effective drug safety associate job description, begin by listing detailed duties, responsibilities and expectations. We have included drug safety associate job description templates that you can modify and use. Sample responsibilities for this position include: Identify out of scope activities in conjunction with the MSS Functional...

**Roles & Responsibilities of Drug Safety Associate or Pharmacovigilance Associate** A Drug Safety Associate is a professional who works in the field of pharmacovigilance within a pharmaceutical, biotechnology, medical company or life sciences consulting firm. The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices...

Company Description We are PrimeVigilance part of Ergomed PLC a specialised mid-size pharmacovigilance service provider established in 2008 We are proud to have achieved global organic growth year after year with staff based across Europe North America and Asia all covering services within Medical Information Pharmacovigilance Regulatory Affairs and Quality...