Principal Medical Writer - Rahway

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

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 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 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 ...

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 ...

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

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) ...

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

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

+ 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 ...

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 ...

Dice is the leading career destination for tech experts at every stage of their careers. · ...

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 ...

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. · ...

FULLY REMOTE · Must Have Experience · 4 year degree · Need to be able to author independently (2+ years authoring) · Experience with CSPs, CSRs, IBs, ICFs, supporting regulatory documents · Must have Veeva RIM experience · CNS experience · Job Title: Medical Writer · Job Descript ...

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 ...