Location: Princeton, NJ, US
Job Summary:
Job Duties
- Provide Risk Management Plan (RMP) support for investigational and marketed products.
- Collaborate with cross-functional teams on risk management strategy.
- Oversee implementation of risk minimization activities.
- Contribute to the creation and tracking of RMP-related documentation.
- Support regulatory inspections, audits, and training on RMPs.
Required Skills
- Knowledge of international RMP regulatory guidelines.
- Proficiency in Document Management Systems and Microsoft Office.
- Excellent communication, organizational, and time management skills.
- Strong collaborative and problem-solving abilities.
Required Experiences
- Minimum 6 years of pharmacovigilance experience.
- Experience in supporting RMPs for investigational and marketed products.
- Background in the pharmaceutical industry, preferably with a relevant healthcare degree.
Job URLs: