Quality Control Medical Writer - San Francisco

Fishawack has an immediate need for a Medical Writer or Sr. Medical Writer who will work in our San Francisco office. Both positions require experience in medical communications or medical education agency. · ...

This position will lead scientific writing activities for development projects and ensure full life-cycle support from clinical study protocols through regulatory submission. · Manages all clinical writing activities outlined in the Project Clinical Development Plans · Reviews do ...

This position is responsible for drafting and managing the content and reviews of clinical regulatory documents for Revolution Medicines products in various drug development phases. · ...

The Medical Writer II will define scope of quality control activities with document authors and source documents. They will conduct independent quality control reviews of documents to ensure accuracy. · ...

Revolution Medicines is seeking a motivated individual with clinical regulatory writing background to play critical role in successful preparation of high-quality submission-ready clinical research documents. · ...

Job summary · An emerging biotech company with a transformative approach to drug discovery is seeking an experienced Senior Medical Writer to join its Regulatory Affairs team. · ...

The Medical Writer 1 applies basic to intermediate documentation preparation and document project management skills to assist in the development, drafting, review, editing and finalization of documents used in conducting clinical studies and reporting clinical study results for r ...

The Medical Writer 1 applies basic to intermediate documentation preparation and document project management skills to assist in the development, · drafting, · reviewing, · editing · and finalizing documents used in conducting clinical studies and reporting clinical study results ...

The Medical Writer assists in the development and drafting of documents used in conducting clinical studies and reporting results. This includes protocols, informed consent forms, and clinical study reports. · Responsibilities:Drafts and edits documents for clinical studies. · Ma ...

The Senior Manager Medical Writer will lead the preparation of clinical and regulatory documents. · ...

+The Senior Manager Medical Writer (QC) will lead the preparation of clinical and regulatory documents. · This role requires adherence to global and regional regulatory guidelines and company standards. · +Lead the preparation of clinical and regulatory documents in accordance wi ...

The Senior Manager Medical Writer (QC) will lead the preparation of clinical and regulatory documents including protocols investigator brochures safety updates clinical study reports and various submission documents.This role requires adherence to global and regional regulatory g ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. · Drafts and manages content and reviews of clinical regulatory documents for Revolution Medicines products in v ...

+Job summary · Develops medical writing function in alignment with Development Sciences department requirements. · +ResponsibilitiesDrafts and edits documents used in conducting and reporting results of clinical studies. · ...

BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. · ...

We are seeking a Senior Medical Writer to join our team at Revolution Medicines. As a key member of our medical writing group, you will be responsible for drafting and managing the content and reviews of clinical regulatory documents for our products in various drug development p ...

Aplica avances en la preparación documental y gestión de proyectos documentales para ayudar a desarrollar, redactar, revisar, editar y finalizar documentos utilizados al realizar estudios clínicos y reportes de resultados de estudios clínicos con fines regulatorios e informes pub ...

We are seeking a Senior Medical Writer to join our team at Revolution Medicines. As a key member of our medical writing team, you will be responsible for drafting and managing the content and reviews of clinical regulatory documents for Revolution Medicines products in various dr ...

Sutro Biopharma is looking for a Senior Medical Writer who will provide leadership in development and execution of document deliverables intended to support clinical trial applications including Health Authority interactions and filings. · Authors complex documents compliant with ...

A Bay Area biopharma focused on next-generation biologics is seeking a seasoned Medical Writer to take a lead role in drafting and managing clinical and regulatory documents. · ...