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Senior Medical Writer

  • Senior Medical Writer job type Posted on: Oct 25, 2026
  • Senior Medical Writer experience level BioPhase
  • Senior Medical Writer employment type Remote, Remote
  • Senior Medical Writer salary Salary: $10 per hour
  • Senior Medical Writer employment type Remote
  • Senior Medical Writer salary Full-time

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Job Title :

Senior Medical Writer

Job Type :

Full-Time

Job Location :

Remote Remote United States

Remote :

Yes

Jobcon Logo Job Description :

BioPhase Solutions specializes in recruiting top talented professionals for the San Diego County Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech company.Responsibilities• Partner cross-functionally with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear, high-quality regulatory documents• Lead and/or contribute to the preparation of clinical and regulatory deliverables, including CSRs, IBs, protocols, briefing documents, and Module 2 summaries• Drive consistency in messaging, structure, and scientific accuracy across documents, including facilitating data interpretation and review discussions• Oversee and/or support document timelines, ensuring efficient review cycles, comment resolution, and on-time submission readiness• Ensure all deliverables align with global regulatory standards (FDA, EMA, ICH), including QC review and collaboration with QA and Regulatory Operations• Contribute to regulatory submissions (IND/NDA), including supporting responses to health authority inquiriesRequirements• At least 10+ years of medical writing experience within sponsor pharma or biotech• Advanced degree required• Demonstrated experience developing regulatory documents, with strong exposure to CSRs and IBs• Extensive experience with owning, contributing to or supporting NDA regulatory submissions• Background in small molecule drug development required• Working knowledge of FDA, EMA, and ICH guidelines (including ICH E3 and E6)• Strong ability to interpret scientific data and communicate it clearly in a regulatory context• Proven ability to manage multiple deliverables and collaborate effectively in a fast-paced environment• Proficiency in Microsoft Office and Adobe; familiarity with Veeva or eCTD systems is a plus• Ability to work remotely while aligning with West Coast hours, with occasional travel as neededWhat we offer:As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.· Full support and career-development resources to help you reach your potential· A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and actApply now and let's make work better!www.biophaseinc.com

Jobcon Logo Position Details

Posted:

Oct 25, 2026

Reference Number:

10440_4476863418

Employment:

Full-time

Salary:

$10 per hour

City:

Remote

Job Origin:

APPCAST_CPC

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BioPhase Solutions specializes in recruiting top talented professionals for the San Diego County Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech company.Responsibilities• Partner cross-functionally with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear, high-quality regulatory documents• Lead and/or contribute to the preparation of clinical and regulatory deliverables, including CSRs, IBs, protocols, briefing documents, and Module 2 summaries• Drive consistency in messaging, structure, and scientific accuracy across documents, including facilitating data interpretation and review discussions• Oversee and/or support document timelines, ensuring efficient review cycles, comment resolution, and on-time submission readiness• Ensure all deliverables align with global regulatory standards (FDA, EMA, ICH), including QC review and collaboration with QA and Regulatory Operations• Contribute to regulatory submissions (IND/NDA), including supporting responses to health authority inquiriesRequirements• At least 10+ years of medical writing experience within sponsor pharma or biotech• Advanced degree required• Demonstrated experience developing regulatory documents, with strong exposure to CSRs and IBs• Extensive experience with owning, contributing to or supporting NDA regulatory submissions• Background in small molecule drug development required• Working knowledge of FDA, EMA, and ICH guidelines (including ICH E3 and E6)• Strong ability to interpret scientific data and communicate it clearly in a regulatory context• Proven ability to manage multiple deliverables and collaborate effectively in a fast-paced environment• Proficiency in Microsoft Office and Adobe; familiarity with Veeva or eCTD systems is a plus• Ability to work remotely while aligning with West Coast hours, with occasional travel as neededWhat we offer:As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.· Full support and career-development resources to help you reach your potential· A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and actApply now and let's make work better!www.biophaseinc.com

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