Job Summary
The Senior Pharmacovigilance Scientist is responsible for overseeing the assessment of safety data, identifying potential signals, and managing risks throughout the lifecycle of pharmaceutical products. This role involves working closely with various cross-functional teams to offer scientific insights for regulatory submissions and support in clinical development initiatives.
Responsibilities
- Lead the evaluation of safety data and signal detection processes.
- Manage risk assessment functions associated with pharmaceutical products.
- Collaborate with cross-functional teams to deliver scientific expertise for regulatory compliance.
- Support clinical development with specialized knowledge in pharmacovigilance.
Qualifications
- Bachelor’s degree in pharmaceutical sciences, nursing, or biological sciences; preference for candidates with degrees in medicine or pharmacy.
- A minimum of 7 years of experience in pharmacovigilance within the pharmaceutical industry.
- At least 3 years of experience in a scientist role or its equivalent.
CSL provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
