Remote Senior Protocol Medical Writer | Regulatory & Clinical
Syneos Health Inc
Syneos Health in Canada/US remote role seeks a Sponsor Dedicated Protocol Medical Writer II/Sr to lead medical writing deliverables across studies. You’ll coordinate multi-department activities, ensure regulatory compliance, and mentor junior writers. Responsibilities include drafting protocols, CSRs, and submissions, reviewing statistical outputs, and maintaining quality under timelines. Strong knowledge of FDA/ICH guidelines and AMA style is essential; remote collaboration across geographies #J-18808-Ljbffr
$80.6k - $175.7k
Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs) Updated: Today Location: Remote, MO, United States Job ID: 25112637 Description Senior Medical Writer... ...meetings. Adheres to established regulatory standards, including, but not...Remote workSeniorRegulatoryContract workFlexible hours- ...Job Description Senior Medical Writer - Clinical Development \n \n Immix Biopharma... ...\n \n United States / Remote / LA, CA \n \n Our 3... ..., reviewing, and editing regulatory documents required for... ...Applications (BLA), study protocols, clinical study reports, and...Remote workSeniorRegulatoryOdd job
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- ...Health, Inc. is seeking a Senior Medical Writer (FSP) with proven experience in clinical document writing, including protocols, CSRs, and IBs. The role emphasizes meeting regulatory standards while delivering... ...schedule. The position supports remote work with flexibility...Remote jobSeniorRegulatory
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- ...Sponsor Dedicated Protocol Medical Writer II/Sr - US/Canada Remote Based Syneos Health® is a leading fully-integrated... ...and accelerate progress. Our Clinical Solutions team members act with a... ...meetings. Adheres to established regulatory standards, including, but not limited...Remote workSeniorRegulatoryContract work
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Terumo Group is seeking a Sr. Medical Writer for a remote role in Los Angeles. This position involves collaborating with clinical and regulatory teams to produce a range of medical documents... ...evaluation reports and study protocols. The salary range for this position...Remote workSeniorRegulatory- ...Therapeutics is a patient-centered, clinical-stage biopharmaceutical company... ...diseases. We are seeking a Senior Manager, Medical Writer to provide regulatory medical writing support for development... ..., leading FDA briefing packages, protocol synopses, and #J-18808-LjbffrRemote workSeniorRegulatory
- ...leading healthcare intelligence and clinical research organization, is seeking a Senior Principal Medical Writer to lead development of high-quality clinical and regulatory documents. The role requires... ...improvements while working in a remote environment. #J-18808-LjbffrRemote workSeniorRegulatory
- ...foundational AI lab to find experienced senior medical writers who can help train their... ...candidates with 5+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate,... ...clinical study reports, protocols, investigator brochures, regulatory...Remote workSeniorRegulatory
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- ...company, in Irvine, CA, seeks a Senior Medical Writer to develop CERs and PMS reports for EU MDR and global regulatory standards. You will design... ...across Scientific Affairs, Clinical Research, Regulatory... .... You will interpret study protocols and results to support clinical...SeniorRegulatory
- ...MMS, a data-focused clinical research organization, seeks an experienced Medical Writer to join a remote, globally oriented team. You will critically... ...literature, write clinical protocols and study reports, and ensure high-quality regulatory submissions. The role...Remote workSeniorRegulatory
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- ...and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will take ownership... ...functional teams in a remote environment. Key... ..., including protocols, clinical study reports... ...brochures, and regulatory submissions Collaborate...Remote workSeniorRegulatoryFull time
- ...is seeking an organized medical writer to lead planning and preparation of high-quality regulatory documents for clinical development. You will collaborate... ...Management to produce protocols, study reports,... ...timelines. The role is fully remote in the United States with...Remote workSeniorRegulatory
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$142k - $153k
...Veristat in the United States is seeking a Principal Medical Writer to independently plan and prepare regulatory documents and medical communications across... ...working with cross-functional teams. This role offers remote work options, a competitive salary range of $142K–...Remote workSeniorRegulatory- ...INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home based anywhere in the US. The ideal... ...role includes creating deliverables like clinical protocols, IND submissions, and more, adhering to...Remote workSeniorRegulatoryWork from home
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- ...are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San... ...Partner cross-functionally with Clinical Development, Biostatistics, and Regulatory teams to translate complex... ..., including CSRs, IBs, protocols, briefing documents, and Module...Remote workSeniorRegulatoryWork at office
$78k - $156k
...and products in diagnostics, medical devices, nutritionals and... ...on-site opportunity for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides... ...files, Clinical Evaluation Protocols, Clinical Evaluation...SeniorRegulatoryWork experience placementWorldwideShift work- ...Global Laboratories is seeking a Medical Writer to interpret complex protocols and prepare study-specific... ...finalize documents used in clinical studies, ensuring regulatory compliance and high-quality scientific... .... The role is remote (East Coast) with standard hours...Remote workRegulatory
- ...Health is seeking a Sponsor Dedicated Protocol Medical Writer II to support remote-based work from Portugal, the UK,... ..., amendments, and related regulatory documents with strict adherence to... ...guidelines. You will collaborate with clinical scientists, manage writing deliverables...Remote workRegulatory
- ...TransPerfect is seeking a senior medical writer to lead the planning and... ...of high-quality regulatory documents across Clinical Development, Regulatory,... ...client teams to deliver protocols, reports, and brochures... ...degree or higher. Fully remote in the US with on-site client...Remote workSeniorRegulatory
- ...individual for our medical writing team. Theseniormedical writer will partner cross-functionallywith... ...Development, Clinical Operations,Biostatistics,Regulatory, and Program... ...underbrisktimelines. Location: Fully remote in the US, but must... ...study reports, protocols, protocol amendments...Remote workSeniorRegulatoryLocal area
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