- Philips (Stamford, CT)
- …Senior Medical Writer will be responsible for authoring and maintaining clinical and post-market documentation (CEPs, CERs, PMCFPs, and PMCFRs). This person may ... Medical Writer - Sleep & Respiratory Care** The...also contribute to our author other technical documents that support Clinical , Regulatory, Risk Management,… more
- Merck (Rahway, NJ)
- …disclosure, and data sharing with external researchers. The Specialist (Disclosure Medical Writer ) will be primarily responsible for preparing clinical study ... (ie, Clinical Study Reports, Protocols, etc.). + Experience in technical or medical writing, familiarity with clinical research documents preferred.… more
- Merck (Rahway, NJ)
- …scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical /scientific and regulatory documents. + Partners with Study Manager ... **Job Description** **Position Description:** **Associate Director, Clinical Scientist** This position drives scientific planning, strategy and execution of Phase… more
- TEKsystems (New York, NY)
- …to permanent position based on performance. The developer will be highly technical , and mentor others on their code and reporting capabilities. The principal ... Epic It would be extremely beneficial for the report writer to be familiar with business objects tools such...for, and write individual reports to support the many clinical /financial modules * Have a clear understanding of Reporting… more