Pharmacovigilance Senior Specialist
Full-time
Metacom Careers
Description - Monitor and assess adverse drug reactions and safety signals.
- Conduct safety case processing and maintain accurate documentation.
- Utilize Veeva Safety Database and Argus for data management and reporting.
- Prepare safety reports and submit to regulatory authorities.
- Collaborate with cross-functional teams to ensure compliance with safety regulations.
Requirements
- Educational Qualifications: Bachelor's degree in Life Sciences or a related field
- Experience Level: 2-5 years of experience in pharmacovigilance
- Skills and Competencies: Proficiency in safety case processing, Veeva Safety Database, and Argus
- Qualities and Traits: Strong analytical skills and attention to detail
- Responsibilities and Duties: Knowledge of regulatory requirements and guidelines
- Working Conditions: Comfortable working in a fast-paced, deadline-driven environment
Vacancy posted 7 days ago
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