Associé Bilingue de la Pharmacovigilance, Bilingue- Opportunité Future / Bilingual Drug Safety [...]

Cencora; Ontario; On-site; CAD 55,000 - 75,000; Full time

Job summary

Cencora is seeking a Bilingual Drug Safety Associate for a future opportunity. The role involves documenting clinical information, collaborating with clients, and ensuring compliance with pharmacovigilance guidelines. Ideal candidates will have a college diploma in Life Sciences and relevant experience in medical information or drug safety. Join a company dedicated to improving health globally and enjoy competitive compensation and benefits.

Benefits

Health Benefits

Wellness Programs

Family Support

Training and Development

Qualifications

• 1-3 years in medical information, clinical research, or drug safety.
• Knowledge of pharmacovigilance guidelines (Health Canada, FDA, EMEA, ICH).

Responsibilities

• Receive, scan, and document clinical information compliant with SOPs.
• Collaborate with clients for additional information or clarifications.
• Prepare reports and handle transcription, translation, and data clarification tasks.

Skills

Analytical Skills

Problem-Solving

Communication

Interpersonal Skills

Organizational Skills

Education

College Diploma in Life Sciences

Tools

MS Office

Job description

Join to apply for the Associé Bilingue de la Pharmacovigilance, Bilingue - Opportunité Future / Bilingual Drug Safety Associate - Future Opportunity role at Cencora .

Our team members are at the heart of everything we do. At Cencora, we are committed to creating healthier futures. If you want to make a difference in health, join our innovative company and help improve lives globally. Apply today!

This is a future job opportunity. If you are interested but do not see a current opening, submit your CV for consideration for future bilingual (French-English) roles. Only qualified candidates will be contacted.

Main Functions and Responsibilities

• Receive, scan, and document clinical information compliant with SOPs and laws.
• Collaborate with internal and external clients for additional information or clarifications.
• Review source data documents and triage adverse event and product quality complaint information.
• Enter data into specific databases and perform quality checks.
• Sort and file incoming documents.
• Assist with source data verification and literature review for safety information.
• Prepare reports and handle transcription, translation, and data clarification tasks.
• Participate in non-conformance and CAPA processes.
• Perform other duties as assigned, including on-demand or standby work.

Experience and Education Requirements

• Minimum college diploma, preferably in Life Sciences.
• 1-3 years in medical information, clinical research, or drug safety, or related pharmaceutical experience.
• Knowledge of pharmacovigilance guidelines (Health Canada, FDA, EMEA, ICH).
• Bilingual in English and French is an asset.
• Ability to work flexible shifts between 8 am and 8 pm.

Skills and Competencies

• Strong analytical and problem-solving skills.
• Effective communication and interpersonal skills.
• Organizational skills with attention to detail.
• Proficiency in MS Office and good internet connectivity for remote work.

What Cencora Offers

Competitive compensation, benefits, and a supportive, inclusive culture. Benefits include health, wellness, family support, training, and development programs.

Equal Opportunity and Accessibility

Cencora is committed to diversity and inclusion, providing accommodations for applicants with disabilities during the hiring process upon request.