Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology)
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Job Location:
Boston, NH - USA
Monthly Salary:
Not Disclosed
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
Overview
The Director of Drug Safety & Pharmacovigilance provides strategic and handson leadership for pharmacovigilance activities supporting aclinicalstage biotech pipeline in inflammatory and oncology diseases. This role is responsible for establishing and executing global safety strategy across early and midstage clinical programs with particular focus on immunemediated toxicities oncology risk management and complex benefitrisk assessment. The Director partners closely with Clinical Development and Regulatory teams to integrate safety considerations into study design dose escalation and development decisions.
Responsibilities
- Develop implement and lead pharmacovigilance strategy for inflammatory and oncology programs across Phase IIII clinical development.
- Provide expert safety guidance related to immunemediated adverse events cytokinerelated toxicities infection risk malignancy risk and oncologyspecific safety concerns.
- Support doseescalation and cohortexpansion decisions including participation in Dose Escalation Committees and Safety Review Committees.
- Maintain ongoing benefitrisk assessments reflecting disease severity unmet medical need and evolving clinical data.
- Serve as the primary safety partner to Clinical Development contributing to protocol design safety monitoring plans stopping rules and risk mitigation strategies.
- Chair or actively participate in Safety Management Teams (SMTs) Joint Safety Forums and other governance bodies.
- Identify emerging safety signals and ensure appropriate escalation through internal safety governance pathways.
- Oversee intake medical review and regulatory submission of Individual Case Safety Reports (ICSRs).
- Ensure highquality MedDRA coding oncologyappropriate event characterization and robust safety safety review meetings and oversee followup of serious and immunemediated adverse events.
- Oversee literature surveillance and safety data collection from investigators sites and vendors.
- Lead development and lifecycle management of developmentstage Risk Management Plans (RMPs) DSURs and safety sections of IBs protocols ICFs and clinical study reports.
- Provide safety input to regulatory submissions (IND/CTA) amendments and responses to health authority questions.
- Support aggregate safety analyses and signal detection activities relevant to oncology and inflammatory disease development.
- Build and maintain fitforpurpose pharmacovigilance operations suitable for a clinicalstage biotech.
- Manage PV vendors and CROs supporting case processing literature review and safety reporting.
- Define and maintain safety database strategy (e.g. Argus or equivalent) ensuring scalability as programs advance.
- Establish pragmatic KPIs and processes aligned with developmentstage needs.
- Ensure inspection readiness for developmentstage regulatory inspections.
- Lead development and maintenance of PV SOPs work instructions and training programs.
- Partner with Quality and Regulatory teams to address safety findings deviations and corrective actions.
- Collaborate closely with Clinical Development Regulatory Affairs Medical Affairs Biostatistics Data Management and Medical Writing.
- Promote a culture of patient safety scientific rigor and informed risktaking appropriate for serious inflammatory and oncology indications.
Qualifications
- Bachelors degree in a scientific or healthcarerelated discipline required advanced degree (MS PharmD PhD MD RN) strongly preferred.
- 12 years of pharmacovigilance or drug safety experience in pharmaceutical or biotechnology settings.
- Direct experience supportingoncology I/O and/or inflammatory disease clinical programs.
- Experience with earlyphase development dose escalation and complex safety decisionmaking.
- Prior involvement in safety governance and regulatory interactions during development.
- Strong knowledge of global PV regulations and guidelines (FDA EMA ICH GCP).
- Experience with safety databases (Argus or equivalent).
- Deep understanding of immunemediated and oncologyspecific safety risks.
- Ability to operate strategically while remaining handson in a lean biotech environment.
Required Experience:
Director
Key Skills
- Hospital Experience
- Acute Care
- Basic Life Support
- ICU Experience
- Infusion Experience
- Triage
- TFS
- Conflict Management
- Nursing
- Critical Care Experience
- Epic
- Medication Administration
About Company
Pioneering Therapies for Cancer and Beyond – Our drug discovery platform is tailored to promote specific protein ubiquitination and subsequent proteasomal degradation of disease-causing, undruggable proteins, in essence leading to pharmacological protein knockout with high efficiency ... View more
