Associate Director, Pharmacovigilance and Patient Safety
192438
Posted: 08/06/2026
- $165,000.00 to $200,000.00
- Research Triangle Park United States
Associate Director, Pharmacovigilance and Patient Safety – RTP, North Carolina
Join a growing biotechnology organization focused on developing innovative therapies for patients with serious and unmet medical needs.
As the Associate Director, Pharmacovigilance and Patient Safety, you will play a critical role in ensuring the integrity, compliance, and effectiveness of PV activities across patient support programs, helping to protect patients while supporting global safety surveillance efforts.
Why Join Us?
We’re seeking an experienced Pharmacovigilance leader with strong expertise in ICSR processing, patient support program oversight, and global safety regulations.
Your Role & Impact
As the Associate Director, you will:
Join a purpose-driven biotechnology company focused on improving and extending the lives of patients worldwide. You'll have the opportunity to shape critical pharmacovigilance processes, collaborate with industry-leading experts, and contribute to innovative therapies that address significant unmet medical needs.
Get in Touch
If this opportunity is of interest, please reach out to Guled Samatar at Meet Life Sciences.
Join a growing biotechnology organization focused on developing innovative therapies for patients with serious and unmet medical needs.
As the Associate Director, Pharmacovigilance and Patient Safety, you will play a critical role in ensuring the integrity, compliance, and effectiveness of PV activities across patient support programs, helping to protect patients while supporting global safety surveillance efforts.
Why Join Us?
- Strategic Leadership Opportunity: Lead PV oversight activities across patient support programs, influencing safety governance and compliance strategies.
- High-Impact Role: Drive safety data exchange processes, inspection readiness, and regulatory compliance while partnering with cross-functional stakeholders.
- Mission-Driven Innovation: Support a company committed to advancing innovative medicines for patients worldwide.
We’re seeking an experienced Pharmacovigilance leader with strong expertise in ICSR processing, patient support program oversight, and global safety regulations.
Your Role & Impact
As the Associate Director, you will:
- Provide strategic leadership for safety data collection, exchange, and oversight across patient support programs
- Ensure compliance with global pharmacovigilance regulations, GVP requirements, and internal quality standards
- Lead safety governance initiatives, inspection readiness activities, and audit management processes
- Oversee adverse event reporting processes, reconciliation activities, and vendor performance management
- Develop and deliver pharmacovigilance training programs to enhance organizational knowledge and compliance standards
- Strong Pharmacovigilance and ICSR
- Knowledge of global GVP regulations and safety compliance
- Experience overseeing patient support programs and call center environments
- Bachelor’s degree in Life Sciences or related field
Join a purpose-driven biotechnology company focused on improving and extending the lives of patients worldwide. You'll have the opportunity to shape critical pharmacovigilance processes, collaborate with industry-leading experts, and contribute to innovative therapies that address significant unmet medical needs.
Get in Touch
If this opportunity is of interest, please reach out to Guled Samatar at Meet Life Sciences.
- Call: 646-582-3675
- Email: guled.samatar@meetlifesciences.com
Guled Samatar
Division Manager
