Senior Director, Regulatory Affairs

Bicara Therapeutics

Senior Director of Regulatory Affairs leading US strategy for oncology development at Bicara Therapeutics. Responsible for global regulatory submissions and team management in a hybrid work environment.

Posted 5/12/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesSenior💰 $275,000 - $315,000 per yearWebsite

About the role

Key responsibilities & impact

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 the 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.

Requirements

What you’ll need

Bachelor's degree in a life sciences discipline required; advanced degree (MS, PharmD, PhD, or MD) preferred.
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; experience with additional ICH regions (e.g., PMDA, Health Canada) strongly preferred.
Proven success leading and preparing teams for health authority meetings and delivering major regulatory submissions (IND/CTA and ideally NDA/BLA/MAA).
Demonstrated ability to manage within a cross-functional matrix; prior people management experience highly preferred.
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.

Benefits

Comp & perks

Health insurance
Dental coverage
Vision coverage
Short term and long term incentives
Cash bonus
Equity incentive opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory strategyregulatory submissionsINDNDABLAhealth authority interactionsoncology developmentICH guidelinesregulatory complianceaudit-ready documentation

Soft Skills

leadershipproject managementcommunicationcollaborationinfluencingorganizational skillsdetail-orientedability to manage prioritiescoachingteam management

Certifications

Bachelor's degree in life sciencesMSPharmDPhDMD