Director, Medical Writing

Position Overview Bicara Therapeutics is seeking a proactive and detail-oriented Director, Medical Writing to lead the development of complex, high-quality scientific documents that support our clinical development and regulatory submissions. Reporting to the VP, Regulatory Affairs, the ideal candidate will work closely with regulatory leadership, cross‑functional teams and external partners to deliver accurate, clear, and compliant documentation on time. This role is ideal for an experienced Medical Writer who thrives in a small, fast‑moving biotech environment. This position is based in our Boston office and follows a hybrid schedule, with three in‑office days each week. Responsibilities Lead the Medical Writing efforts and strategy for clinical and strategic regulatory documents, ensuring high quality and on‑time writing deliverables in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs). This includes but is not limited to health authority briefing packages, pediatric plans, designation requests, clinical protocols, investigator brochures, clinical study reports, and IND/BLA summary documents. Document lead for regulatory document creation, review and approval process. Work with project team members to develop a plan and timelines for regulatory document initiation and completion. Partner with cross‑functional leads to interpret and present nonclinical and/or clinical data in documents for regulatory submission. Contribute to documents for regulatory submission in accordance with applicable regulatory guidelines. Coordinate and drive the adjudication of review comments with other authors and reviewers, and provide timely follow‑up to address outstanding queries or comments until resolution. Copy edit, proofread reviews, and modify documents to ensure organization, clarity, use of language, grammar, scientific standards, and consistency between textual presentations and listings, tabular or graphic displays. Technical editing: Format documents written by others to align with company templates. Review Statistical Analysis Plans and table, listing, and figure shells to determine appropriateness of content for writing. Directly oversee and manage resources to meet writing needs, including flexible use of consulting external writers or internal hires, as appropriate. Ensure training on SOPs/procedures for all writers; provide coaching and mentorship for junior staff. Qualifications Bachelor's degree or higher in life sciences, pharmacy, medicine, or a related field; advanced degree (PhD, PharmD) preferred. 8+ years of relevant writing experience, including critically analyzing and summarizing scientific data. Strong experience authoring clinical and strategic regulatory documents (e.g., briefing packages, fast track/breakthrough designation requests). Experience authoring key clinical summary documents to support NDA/BLA and/or MAA submissions. Knowledge of the drug development process; working knowledge of relevant ICH guidelines and FDA/EMA regulatory requirements. Proficiency with MS Office Suite (Word, Excel, PowerPoint), document management systems, and use of electronic document templates. Core Competencies Exceptional written and verbal communication skills. High attention to detail, including fact‑checking, logic flow and document structure. Ability to work independently and collaboratively in a fast‑paced cross‑functional team environment consisting of internal and external team members. Strong influence management skills as applied to cross‑functional clinical teams. Flexible with changing priorities. Company Overview Bicara Therapeutics is a clinical‑stage biotech company pioneering bifunctional antibodies for targeted tumor modulation. Founded in 2020, we have built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA – a potentially first‑in‑class bifunctional EGFR‑directed antibody combined with a TGF‑β ligand trap. Our innovative approach combines tumor‑targeting with tumor modulation, where one arm localizes to the tumor while the other serves as a modulator, designed to deliver superior efficacy, improved safety, and enhanced durability directly at the tumor site. FICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF‑β‑driven resistance mechanisms – ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. For more information, please visit Here at Bicara, we believe in building diverse teams and cultivating a culture where all voices are included. We encourage people from all backgrounds to apply. Bicara Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Compensation Range: $222K – $258K #J-18808-Ljbffr Bicara Therapeutics