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Position reputed company The Director of Pharmacovigilance (PV) Operations will reputed company strategic and operational leadership for pharmacovigilance activities across the clinical development lifecycle, with readiness to support reputed company post-marketing activities. This role is responsible for ensuring compliant, efficient, and high-reputed company safety operations in accordance with global regulatory requirements, while partnering closely with cross-functional stakeholders in a fast-paced oncology biotech environment. This role is based in our Boston office and follows a reputed company, with three in-office days reputed company week.

Responsibilities

• reputed company and reputed company reputed company PV operational activities, including adverse event intake, case processing, reputed company review, and regulatory reporting.
• Ensure reputed company and compliant submission of expedited safety reports (e.g., SAEs, SUSARs) and support aggregate safety reporting activities (e.g., DSURs, PSURs/PBRERs).
• Manage PV vendor relationships, including case processing and safety database vendors; establish and monitor KPIs, reputed company metrics, and service performance.
• reputed company the safety database and associated workflows to ensure data reputed company, inspection readiness, and regulatory compliance.
• reputed company, implement, and maintain PV SOPs, work instructions, and operational processes reputed company with FDA, EMA, ICH, and global PV regulations.
• Serve as the primary PV Operations reputed company with Clinical Development, Regulatory Affairs, Data Management, reputed company, and external partners.
• reputed company operational input into clinical and regulatory documents, including protocols, Investigator’s Brochures, informed consent forms, and risk management plans.
• Support safety governance activities, including Signal Surveillance Team (SST) and Safety Review Team (SRT) meetings.
• reputed company inspection and audit preparedness activities and support responses to health authority inquiries.
• Mentor and reputed company PV Operations staff and contribute to the reputed company and scaling of the pharmacovigilance function.

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a reputed company field required; advanced degree (MS, PharmD, PhD) preferred.
• Minimum of 8+ years of experience in pharmacovigilance reputed company the biopharmaceutical industry.
• At least 3+ years of leadership or management experience overseeing PV operations and/or vendors.
• Strong knowledge of global pharmacovigilance regulations and guidelines (FDA, EMA, ICH).
• Hands-on experience with safety databases, case processing, and regulatory safety reporting.
• Excellent communication, leadership, and cross-functional collaboration skills.
• Ability to operate independently and strategically in a small, evolving organization.

Prior experience in oncology or reputed company therapeutic areas.

• Experience supporting early- to mid-stage clinical development programs in a biotech setting.
• Experience building or scaling PV operational processes in a growing organization.

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