Senior Medical Writer

Job is Expired
Location: Remote
Compensation: To Be Discussed
Reviewed: Tue, Mar 24, 2026

Job Summary

A company is looking for a Senior ICF Writer (Remote).

Key Responsibilities
  • Critically evaluate and interpret medical literature for study design and scientific rigor
  • Write and edit clinical development documents, including Informed Consent Forms and Clinical Protocols
  • Mentor medical writers and manage the production of interpretive guides


Required Qualifications
  • At least 3-5 years of regulatory writing and clinical medical writing experience in the pharmaceutical industry
  • Bachelor's, Master's, or Ph.D. in a scientific, medical, or clinical discipline
  • Experience with informed consent and clinical study protocols as a lead author
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines
  • Expert proficiency in MS Word, Excel, and PowerPoint

COMPLETE JOB DESCRIPTION

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