Remote Life Sciences Job at Cencora, Canada | Apply Online For Drug Safety Associate Role
Interested in how safety information is collected, reviewed and reported after patients receive treatment? This remote life sciences job at Cencora involves supporting adverse event reporting, reviewing clinical information and maintaining accurate safety records. The Cencora drug safety associate contract is full-time, runs six months and is listed as remote in Ontario, Canada, within the Innomar Strategies business.
- Position: Drug Safety Associate
- Location: Remote, Ontario, Canada
- Job ID: R2618674
About The Company
Cencora is a global healthcare company focused on improving the lives of people and animals. This role supports its Canadian patient and provider support and pharmaceutical commercialization services, marketed through Innomar Strategies.
Remote Life Sciences Job: Role Overview
In this Cencora drug safety associate role, the associate will process clinical and safety information according to standard operating procedures, client protocols and applicable requirements. Responsibilities include adverse event documentation, product quality complaint processing, report quality checks and follow-up activities.
The role also involves communicating with internal and external clients to clarify information and help maintain complete, accurate safety records.
Key Responsibilities
- Receive, scan and document clinical information in accordance with procedures and applicable legislation.
- Review source documents and triage adverse events and product quality complaints.
- Enter and submit safety information into program-specific databases.
- Request missing information and prepare follow-up letters and data clarification requests.
- Perform quality checks on adverse event reports and assist with source data verification.
- Screen medical and scientific literature for safety information.
- Prepare reconciliation reports and support transcription, translation and redaction activities.
- Organize incoming documents and participate in non-conformance and corrective and preventive action (CAPA) processes.
Education and Experience
- Minimum education: College-level education.
- Strong asset: A diploma or degree with a concentration in life sciences.
- Experience: One to three years in Medical Information, Clinical Research or Drug Safety, or equivalent related experience in pharmacy or pharmaceutical fields.
- Knowledge of pharmacovigilance guidelines from Health Canada, the US FDA, EMEA and ICH.
- Medical terminology knowledge is an asset.
- Bilingual proficiency in English and French is an asset.
Cencora Drug Safety Associate Skills and Remote Work Requirements
Candidates for the Cencora drug safety associate role should bring strong analytical, organizational and problem-solving skills, with careful attention to detail and the ability to meet deadlines. Clear communication, effective teamwork and adaptability are also important.
Proficiency in Microsoft Office applications is expected, and a reliable internet connection is required for remote work.
Compensation and Benefits
A salary range is not specified in the supplied posting. Cencora describes health and wellness benefits, family support resources, training, professional development and mentorship opportunities. Applicants should confirm which benefits apply to this six-month contract.
Application Details
- Work arrangement: Remote, listed for Ontario, Canada.
- Contract duration: Six months.
- Working hours: Full-time.
Accurate safety reporting helps teams understand and respond to potential risks associated with medicines. This remote life sciences job offers the opportunity to apply your clinical research, pharmacy or drug safety experience to that work. If you bring careful documentation skills and relevant pharmacovigilance knowledge, consider applying for Cencora’s six-month opportunity.
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