Exec Medical Director, Pharmacovigilance Risk Management

This is a fully remote position, open to applicants in United States.

📋 Description

• Formulate and implement the global product safety strategy for clinical development initiatives.

• Oversee safety surveillance efforts and risk management projects.

• Develop strategies for analyzing safety data across clinical trials.

• Present safety information to key stakeholders, including Health Authorities.

• Create risk management plans to ensure product effectiveness.

• Provide mentorship to junior team members and train staff on safety protocols.

⛳️ Requirements

• M.D. degree with a minimum of 10 years of post-residency experience; or an equivalent mix of education and experience.

• At least 3 years of clinical experience post-residency.

• Board Certification (if within the US) is preferred.

• A minimum of 10 years of pharmacovigilance experience or relevant experience in a pharmaceutical or biotechnology firm.

• Significant clinical experience in oncology is advantageous.

• Prior experience in project and team leadership/management is preferred.

• Strong knowledge and comprehension of US and EU pharmacovigilance regulatory requirements and general regulatory expectations.

🏝️ Benefits

• 401k plan with generous contributions from the company.

• Group medical insurance coverage.

• Dental and vision insurance.

• Life insurance coverage.

• Disability insurance options.

• Flexible spending accounts available.

• Discretionary annual bonus program.

• Sales-based incentive plan for field sales personnel.

• Opportunities to purchase company stock.

• Long-term incentive programs.

• 15 accrued vacation days during the first year.

• 17 paid holidays, including a company-wide winter shutdown in December.

• Up to 10 sick days allowed throughout the calendar year.