Senior Medical Writer — Clinical Documents Lead

Full time The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker...

IQVIA is seeking a senior Medical Writer to deliver high-quality clinical documents for eye health and inflammatory indications. You will integrate with sponsor teams, manage timelines, and ensure adherence to regulatory requirements across ICH, FDA, and EMA guidelines. The role emphasizes senior-level writing leadership, collaboration across disciplines,...

Full time The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker...

As part of one of the world’s most prestigious healthcare advertising agencies, CDM Barcelona brings people, brands, ideas and innovation together to change real lives in extraordinary ways. Our core values allow us to work with clients in a way that changes their perception of what an agency can and should be. We lift each other up, challenge...

Principal Medical Writer is responsible for the development of clinical documents for submissions to regulatory authorities globally.Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures (IBs), Clinical Study Reports (CSRs), and marketing authorization submission...

Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs)Updated:Yesterday |Location:Remote, Spain |Job ID:********-OTHLOC-******DMAD-2DRDescriptionSenior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs)Syneos Health® is a leading fully integrated life sciences services organization...

Principal Medical Writer is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization...

## Medical Director, Clinical Development Hematology Barcelona, , Spain Apply Now Find out how well you match with this job**This is what you will do:**The Medical Director, Clinical Development, may lead or support the clinical subteam and the global program team to construct global clinical development plans and contribute to the development of asset level...

IQVIA is seeking a senior-level FTE Medical Writer to deliver clinical documents across CTRs, protocols, IBs and submission materials with emphasis on eye health and inflammation.The role embeds in sponsor processes, aligning with project teams, timelines, and required trainings.The ideal candidate has ~5 years of medical writing in biopharma or CROs, strong...