About ORIC Pharmaceuticals
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. Backed by Correlation Ventures.
About the role
The anticipated base salary for Vice President level candidates who will work on-site at our San Diego location is between $310,000-$385,000 per year. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- MD, DO, PharmD, PhD, or equivalent advanced scientific/healthcare degree
- 12+ years of progressive experience in pharmacovigilance, clinical safety, or drug development within the biotechnology or pharmaceutical industry
- Significant experience leading and managing a pharmacovigilance or patient safety function or team
- Demonstrated experience supporting investigational products across Phase 1-3 clinical development
- Deep knowledge of global pharmacovigilance regulations and guidelines, including FDA, EMA, ICH, and GCP requirements
- Experience with safety governance, benefit-risk assessment, signal detection, risk management plans, and inspection readiness
More about this role
- Develop and execute ORIC’s global pharmacovigilance strategy in alignment with corporate objectives and applicable regulatory requirements
- Provide leadership for benefit-risk evaluation, safety surveillance, signal detection, signal management, and risk management across ORIC’s investigational products
- Own all medical safety aspects of clinical development, including safety input into protocols, Investigator Brochures, clinical study reports, and regulatory submissions
- Lead the strategy for and drive safety-related content for protocols, Investigator Brochures, DSURs, PSURs, risk management plans, informed consent forms, reference safety information, clinical study reports, and regulatory filings
- Serve as a senior safety advisor to the Chief Medical Officer and represent Pharmacovigilance in governance committees and safety review meetings
- Establish and evolve scalable pharmacovigilance systems, processes, quality frameworks, and vendor partnerships to support a growing oncology portfolio
- Partner with Clinical Development, Biostatistics, Regulatory Affairs, and Medical Affairs to lead and validate safety signal assessments
- Communicate emerging safety information to...
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