Opportunity Overview
Are you passionate about enhancing patient safety and ensuring compliance within the life sciences industry? This is a unique chance to leverage your expertise in a collaborative environment dedicated to strengthening global pharmacovigilance programs and safeguarding patient outcomes.
Key Responsibilities
- Oversee and manage essential pharmacovigilance activities, ensuring alignment with safety regulations and corporate objectives.
- Focus on vendor management, patient safety programs, and the development of safety systems.
- Manage patient safety vendor relationships, including Patient Support Programs, Market Research Programs, call centers, and digital health initiatives.
- Review and negotiate contracts while ensuring adherence to Pharmacovigilance Agreement (PVA) requirements.
- Oversee the reconciliation of safety information and quality control activities in collaboration with suppliers and corporate partners.
- Support the development and maintenance of the Pharmacovigilance System Master File (PSMF).
- Ensure the accuracy and completeness of data collection programs and associated PVAs within the Global Patient Safety PV Oversight System.
Qualifications
- Bachelor's degree in a medical or life sciences field or an equivalent healthcare professional qualification (e.g., RN, RPh).
- Proven experience in pharmacovigilance or drug safety with a strong understanding of safety reporting and compliance.
- Exceptional organizational skills and meticulous attention to detail.
- Strong project management capabilities, with the ability to manage multiple priorities and meet deadlines effectively.
- Advanced degree preferred, though not required.
Compensation
Hourly rate: $50.00 - $60.00
Company Profile
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