Cencora is a global leader in the healthcare industry, dedicated to creating healthier futures for people and animals. We are currently seeking a detail-oriented Pharmacovigilance Analyst to join our remote team and contribute to our mission of improving lives through safety and compliance excellence.
Key responsibilities
- Identify and process Adverse Events, Adverse Drug Reactions, and Medical Device Incidents from source documentation.
- Manage Individual Case Safety Report processing, including triage, data entry, MedDRA coding, and narrative writing.
- Conduct literature reviews and assist in the preparation of aggregate safety reports such as PSURs, PBRERs, and DSURs.
- Perform signal detection activities and contribute to the development and maintenance of Risk Management Plans.
- Collaborate with internal and external stakeholders to ensure accurate data collection and regulatory compliance.
Requirements
- Bachelor's degree in life sciences, pharmacy, chemistry, biomedical sciences, or a related field.
- Minimum of 2 years of experience in regulatory affairs, quality assurance, or compliance.
- Strong understanding of pharmacovigilance processes and regulatory documentation standards.
- Excellent analytical skills with the ability to manage complex safety data and reporting requirements.
What we offer
- Comprehensive health and wellness benefits, including medical, dental, and vision coverage.
- Support for work-life balance through paid parental and caregiver leave, and family building assistance.
- Extensive professional development resources, including training programs and mentorship opportunities.
- An inclusive culture that values diversity and provides equal opportunities for all team members.