Senior Manager Medical Writer - South San Francisco, CA

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. · ...

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 including protocols investigator brochures safety updates clinical study reports and various submission documents.This role requires adherence to global and regional regulatory g ...

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 ...

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 ...

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 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 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 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. · ...

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. · ...

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. · ...

This is a unique opportunity to join a small, high-impact team building AI systems that accelerate drug development and transform how regulatory documents are created reviewed and quality-checked.Review and quality-check AI-generated regulatory content for accuracy compliance and ...

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 ...

+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. · ...

We are seeking a motivated individual with clinical regulatory writing background to play a critical role in the successful preparation of high-quality clinical research documents. · ...

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. · ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. · Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs, CSRs, perio ...

The QMS Technical Writer Temporary is responsible for creating high-quality content. They will interact with individuals at multiple levels within all functional departments to build relationships with partners that manufacture products. · ...

The Entry Writer is responsible for ensuring compliance with customs regulations and facilitating the smooth import and export of goods for the company. · ...