Medical Writer - Rahway

Cella has an exciting opportunity for a Principal Medical Writer at an award-winning, best-in-class, in-house agency at a major pharma company. · Develops and reviews different types of deliverables across diverse project types and audiences. · Deep experience with common medical ...

We have an exciting opportunity for a Principal Medical Writer at an award-winning agency with a major pharma company. This role will support our work with the oncology business unit across established and pipeline products. · Develops and reviews different types of deliverables ...

We have an exciting opportunity for a Principal Medical Writer at an award-winning agency within a major pharma company. · Candidate must be able to draft and review scientifically accurate content for medical clients in oncology and immunology. · Develops and reviews different t ...

We are hiring Medical Writer/Clinical - III (Senior) for one of our clients. · Acts as a capable scientific contributor and subject matter expert in preparation of selected scientific response documents (SRD). · ...

This role requires close working relationships with BCI leadership, · prioritizing scientific publications and related materials that support strategic communication imperatives of WW Patient Safety. · Drafting scientifically accurate content for clients projects. · Writing origi ...

Kelly Science and Clinical FSP is currently seeking a EUMDR Medical Writer for remote engagement with Global Medical Device client. · ...

Kelly Science and Clinical FSP is seeking a EUMDR Medical Writer for a remote long-term engagement with one of our Global Medical Device clients. · This person will join our Kelly FSP (Functional Service Provider) division. · As a Kelly FSP employee you may be eligible for paid ...

Our client is seeking a talented Medical Writer to join their growing international team. · ...

The medical writer will oversee assigned medical writing projects including clinical study protocols reports INDs investigator brochures reviewing informed consent forms · Write edit manage production high-quality clinical documentation for submission to regulatory authorities ...

Marketing Healthcare Writer (part-time, romote) · Location: Morristown, NJ- Remote · Duration: Contract till January 2027 with possibility to extend · Shift: 1st, Monday to Friday · Note: · Shift: 1st Work Schedule: Mon-Fri, 9-5 est , 20-40hrs/week (depending on business needs) ...

The medical writer will be responsible for the management and oversight of assigned medical writing projects. · Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols. · Act as a member of clinical trial teams. · ...

Work directly with clinical study teams in preparation of scientifically valid regulatory documents including protocols and protocol amendments. · ...

The Medical Writer is responsible for contributing to the development of high-quality medical content that meets the client's objectives. This includes derivative content development in collaboration with scientific leads. · ...

Haymarket Media is seeking a Medical Writer to join their PRI team. · ...

Position       : Medical Writer (Must Have EU MDR) · Location : Franklin Lakes, NJ · Duration : 12 Months Contract · Total Hours/week : 40.00 · Description: · The Medical Writer in client Medical Pharmaceutical Systems Medical Affairs is responsible for the generation and develop ...

+ Develop high quality medically accurate content in print or digital format for a wide range of medical communication resources+ Deliver requested projects per established timelines+ Conduct literature reviews and develop annotations to support promotional claims in a variety of ...

The Medical Writer is responsible for contributing to the development of high-quality medical content that meets the client's objectives. · ...

Responsibilities · Develop clinical & regulatory documents (CSRs, CSPs, IBs, ICFs, CTD Modules, NDAs/BLAs/MAAs). · Ensure compliance with ICH, GCP, FDA & EMA guidelines. · Collaborate with Clinical, Regulatory, Biostatistics & Medical Affairs teams. · Manage multiple projects ...

We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory guidelines. · The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, an ...

We're seeking talented Medical Writers with experience in pharmacovigilance to join us Our partners range from emerging biotech firms to established pharmaceutical companies. · Prepare and review pharmacovigilance documents including: · Periodic Safety Update Reports · Risk Mana ...