Medical Writer Consultant

Job Title: Medical Writer Consultant
Company: Biopharma
Location: Remote

Brio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent on an exclusive search basis to the Biopharma, Pharma, Device, and CRO industries. We work on behalf of organizations that value true talent acquisition partners and specialize in supporting emerging Biopharma companies offering life-changing therapies. Our many years of experience, subject matter expertise, comprehensive search process, and genuine passion to deliver rare talent defines Brio.

Position Overview:
We are partnering with an innovative biopharma company focused on advancing targeted oncology therapies. They are seeking a Medical Writer Consultant to support clinical development activities for a PSMA-targeted asset. This contract role will collaborate cross-functionally to generate key regulatory and scientific documents that meet the highest standards of quality and compliance.

Opportunity Highlights:

  • Prepare, revise, and QC clinical and regulatory documents including study protocols, investigator brochures, CSRs, and informed consent forms

  • Draft high-quality scientific content for INDs/NDAs and other regulatory submissions

  • Develop and manage adverse event narratives with clarity and accuracy

  • Maintain consistency in style, format, and terminology across clinical documents

  • Collaborate closely with Clinical Operations, Regulatory, Medical Affairs, and Biomarker teams

  • Contribute to the creation of manuscripts, abstracts, posters, and presentations for scientific publication

Position Requirements:

  • Bachelor’s Degree required; advanced degree (MS/PhD/PharmD) preferred

  • Demonstrated experience in regulatory and scientific writing within a clinical development setting

  • Strong therapeutic area knowledge in Oncology; experience with PSMA-targeted therapies is a plus

  • Proficiency in protocol and narrative writing, as well as submission support

  • Ability to work independently and collaboratively in a fast-paced, cross-functional environment

We welcome the opportunity to provide a full job description upon resume review.