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About this role
OrcaBio is seeking a Director/Head of Pharmacovigilance to lead safety functions and manage a dedicated team, ensuring compliance with safety regulations and overseeing risk management activities.
Description
Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.
Responsibilities
- Lead risk management and mitigation activities for assigned products, leading safety data review and analysis for all products.
- Responsible for providing safety-related content for all clinical and regulatory documents.
- Lead inspection preparedness efforts for pharmacovigilance and represent Orca’s pharmacovigilance organization at regulatory inspections.
- Stay abreast of changes in regulations, leading updates to SOPs and other documentation to address any process gaps.
- Identify and address resource and infrastructure needs, contribute to departmental budgets and planning to align with Orca products’ stage of development.
- Represent product safety in the cross-functional team environment.
- Lead safety governance activities in collaboration with medical monitors and leadership.
- Lead safety related activities for regulatory filings including development of meeting request and briefing book content, SAP and TFL review, signal detection and risk identification, responses to regulatory queries, RMPs, REMs, ISS strategy, and regional safety related labeling activities.
- Provide guidance and mentorship to all direct reports within the pharmacovigilance function, including support and oversight of operations.
Requirements
- Advanced degree in a biologic/medical/clinical/nursing field: Pharmacist/PharmD, Nurse Practitioner, MD, or PhD.
- 10+ years of experience in drug safety, safety science and risk management at a pharmaceutical, biotech, or CRO, including people leadership experience.
- Knowledge of US and EU safety regulations pre and post marketing pharmacovigilance requirements.
- Experience with pharmacovigilance risk management, preferably at a commercial-stage company.
- Proficiency in preparing pre-marketing and post marketing safety regulatory documents, including PSURs, PBRERs, PADER, and Risk Management Plans.
- Experience with clinical development, risk/benefit analysis, and safety assessment.
- Strong clinical, analytical, problem-solving, scientific writing, and communication skills.
- Prior experience working on a BLA/NDA. Prior experience leading risk management activities for a BLA/NDA preferred.
- Hands-on mentality, ability to operate in a small biotech environment.
- Knowledge of cell therapy, bone marrow transplant or hematology oncology is a plus.
- Expertise in analyzing safety data from clinical and safety databases.
- Experience in MedDRA coding and search strategies.
- Excellent independent judgment based on knowledge and expertise.
- Strong personal time management and project management skills.
Conditions & Benefits
- The anticipated annual salary range is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law.
- For remote-based positions, this range may vary based on your local market.
- Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits.
- Other perks include subsidized daily lunches and snacks at our on-site locations.
Job Details
Salary$55,000–$90,000
LocationRemote
AI Score★★★★★★★★☆☆ 8/10
PostedSep 14, 2026 (8d ago)
Tags & Skills
Otherremote