Become a key player in drug safety with Cencora. This full time role focuses on monitoring adverse events and ensuring compliance in our pharma commercialization services in Canada. Cencora is seeking a Drug Safety Associate to support patient and provider initiatives through Innomar Strategies.

The position requires 1-3 years of experience in medical information, clinical research, or drug safety. High attention to detail and excellent communication skills are essential as you analyze data, coordinate with clients, and perform compliance checks. Key Responsibilities:

- Document clinical information following SOP and protocol
- Review data and triage adverse event information
- Enter data into program-specific databases
- Conduct quality checks on safety reports
- Assist in source data verification tasks

Requirements:

- Minimum college education in Life Sciences preferred
- 1-3 years in Medical Information or Clinical Research
- Knowledge of pharmacovigilance guidelines
- Bilingual in English and French is an asset
- Strong analytical and organizational skills

Utilize your expertise in drug safety to enhance healthcare outcomes at Cencora.

📌 Drug Safety Associate at Cencora (Moncton)
🏢 Myhrabc
📍 Moncton