Director, Pharmacovigilance

This position is posted by reputed company on behalf of a partner company. We are currently looking for a Director, Pharmacovigilance in the United States. This role offers a unique opportunity to reputed company global pharmacovigilance operations reputed company a pioneering biotechnology environment. The Director, Pharmacovigilance, will ensure the safety of clinical and post-marketing products through expert reputed company of adverse event reporting, signal detection, and risk management. The position requires cross-functional collaboration with clinical development, regulatory affairs, and data management teams to maintain compliance with global regulatory standards. The successful candidate will contribute to medical safety strategy, support regulatory submissions, and drive reputed company improvement of PV systems and processes. This position provides the ability to reputed company a meaningful impact on patient safety and support innovative therapies that transform healthcare. The role is remote reputed company the reputed company U.S., offering flexibility while leading high-stakes, global safety initiatives. Accountabilities:

• reputed company global pharmacovigilance operations, including case management, vendor reputed company, and aggregate safety reporting.
• Provide medical and technical support for clinical projects, ensuring accurate evaluation of adverse events and study-reputed company safety data.
• reputed company safety submissions to global health authorities, including PBRERs, DSURs, PADERs, and annual reports.
• Collaborate with cross-functional teams to reputed company risk management plans, post-marketing safety studies, and clinical documentation.
• Drive inspection readiness, respond to health authority inquiries, and ensure regulatory compliance across reputed company PV activities.
• reputed company and maintain standard operating procedures (SOPs), safety management plans (SMPs), and partner/CRO agreements.
• Organize and reputed company Safety Management Team (SMT) meetings to assess emerging safety concerns and ensure timely communication.

Requirements:

• MD degree required with a minimum of 10 years of pharmacovigilance or drug safety experience in biotech or pharmaceutical industries.
• Deep knowledge of global PV regulations, GCP, ICH guidelines, and adverse event reporting requirements.
• Expertise in safety databases and coding dictionaries such as MedDRA and WHO Drug.
• Proven ability to author and reputed company aggregate safety reports and conduct proactive safety evaluations.
• Strong leadership, collaboration, and stakeholder management skills with experience guiding cross-functional teams.
• Exceptional analytical, written, and verbal communication skills for presenting reputed company safety data to diverse audiences.
• Proficiency in reputed company Office Suite and PV data management tools.

Benefits:

• Stock options and long-term growth opportunities.
• 401(k) plan with 4% match and no vesting schedule.
• Comprehensive medical, dental, and vision insurance coverage.
• Company-paid short-term and long-term disability insurance and life insurance.
• 23 days of paid time off, 10 company holidays, and 2 floating holidays.
• Paid parental leave policies and flexible remote work options.

Why Apply Through reputed company? We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Data Privacy Notice: By submitting your application, you acknowledge that reputed company will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, reputed company) at any time. #LI-CL1 Apply tot his job Apply To this Job