Senior Director, Regulatory Affairs

Bicara Therapeutics•Boston, MA

21h•Hybrid

About The Position

Bicara Therapeutics is seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory strategy for our biologics pipeline. Reporting to the VP, Regulatory Affairs, you will serve as the primary US regulatory lead with a core focus on BLA strategy and execution — from IND through BLA submission and approval. You will manage a small team of Regulatory Affairs professionals, providing mentorship and oversight while working in close partnership with the VP to ensure alignment on regulatory direction, agency interactions, and submission timelines. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week.

Requirements

Bachelor's degree in a life sciences discipline required
10-12 years of progressive regulatory affairs experience in the biotech or pharmaceutical industry.
Prior oncology/hematology regulatory experience required, with a track record of contributing to oncology development programs across multiple phases.
Demonstrated experience leading global regulatory strategy, including direct engagement with FDA and EMA
Proven success leading and preparing teams for health authority meetings and delivering major regulatory submissions (IND/CTA and ideally NDA/BLA/MAA).
Deep working knowledge of global regulatory requirements, ICH guidelines, and oncology-specific frameworks and expedited pathways (e.g., Breakthrough Therapy, Fast Track, Accelerated Approval, PRIME, orphan drug).
Strong leadership, influencing, and project management skills; comfortable operating within a nimble and fast-paced environment typical of a small, clinical-stage biotech.
Exceptional written and verbal communication skills, including experience presenting to and negotiating with health authorities and senior internal stakeholders.
Detail-oriented, highly organized, and able to manage multiple priorities and competing deadlines.

Nice To Haves

advanced degree (MS, PharmD, PhD, or MD) preferred
experience with additional ICH regions (e.g., PMDA, Health Canada) strongly preferred
Prior people management experience highly preferred

Responsibilities

Develop and execute integrated global regulatory strategies to advance investigational oncology assets from early development through approval and lifecycle management, partnering closely with the VP, Regulatory Affairs.
Serve as global regulatory lead on assigned programs, providing strategic guidance to cross-functional teams (Clinical, Nonclinical, CMC, Biostatistics, Clinical Operations, Medical Affairs, and Commercial).
Lead the planning, preparation, and submission of high-quality regulatory documents to FDA, including INDs, briefing documents, orphan/breakthrough designations, amendments, annual reports, and NDA/BLAs. Collaborate with external vendors for submissions in other regions.
Plan, prepare, and lead health authority interactions, including pre-IND, Type B/C, EOP, and pre-submission meetings; coach and prepare cross-functional teams for successful engagements.
Lead and manage a small US team of regulatory professionals; set priorities, allocate work, and cultivate a collaborative, accountable team culture.
Anticipate regulatory risks across regions and proactively design mitigation strategies; advise on regulatory implications of program decisions.
Monitor and interpret evolving global regulations, ICH guidelines, and oncology-specific policies (e.g., Project Optimus, accelerated approval reform), and translate them into actionable strategy.
Partner with external collaborators, CROs, regulatory consultants, and co-development partners to ensure aligned, efficient execution of global regulatory plans.
Ensure compliance with applicable global regulations and internal quality and SOP requirements; maintain audit-ready regulatory documentation and inspection readiness.