Associate Medical Writer

The Medical Writing Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio. The Assistant Narrative Medical Writer is responsible for the development of medical writing deliverables for a limited set of documents within a single therapeutic area under the supervision of management...

**Job Description**: The Medical Writing Department of the Global Clinical Trial Operations organization prepares a variety of regulated documentation in support of the clinical development portfolio. **The Associate Narrative Medical Writer (MW)** is responsible for the development of medical writing deliverables for a limited set of documents within a...

The Medical Writing Department of the GCTO organization prepares various regulated documentation. The Senior Medical Writer Safety Services role focuses on participant safety reporting, such as participant narratives, that support the clinical and regulatory writing portfolio. The Senior Medical Writer Safety Services is responsible for developing and...

**Job Description**: The Medical Writing Department of the Global Clinical Trial Operations organization prepares a variety of regulated documentation in support of the clinical development portfolio. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and...

**Job Description**: The Medical Writing Department of the Global Clinical Trial Operations organization prepares a variety of regulated documentation in support of the clinical development portfolio. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and...

**Job Description**: The Principal Medical Writer Safety Lead is responsible for development and management of medical writing deliverables, with a focus on safety reporting, such as participant narratives, that support the clinical regulatory writing portfolio.Capable of working independently to achieve goals.In this role the Principal Medical Writer Safety...

**Job Description**: **Primary Responsibilities**: - Prepares selected components of regulatory clinical documentation - Develops knowledge of regulatory medical writing and therapeutic area/investigational product to support pipeline projects - Participates, with supervision, on document-specific teams - Develops competence in writing, editing, and...

Role Summary Medical Science Liaison, Associate Director (MSL AD) is a credentialed therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. The role provides scientific leaders (SLs) balanced, factual, scientific information about non-product areas of interest to the Company and...

**Job Overview** The Evidence Synthesis Associate Consultant will support rigorous analyses and critical appraisals of published medical evidence across a wide range of diagnostic, prognostic, therapeutic, and other clinical interventions, as well as drafting reports. This individual will also provide technical expertise on evidence synthesis methods,...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice is searching for a **Senior Executive-Clinical Regulatory Writing Consultant** to join one of our clients. **Main Job Tasks and...