Bilingual Drug Safety Coordinator - Remote Eligible

Innomar Strategies

Quebec

Hybrid

CAD 50,000 - 52,000

Full time

4 days ago
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Benefits offered by this job

Medical care
Dental care
Vision care
Training programs
Professional development resources
Mentorship programs

Job summary

Innomar Strategies in Canada seeks a Bilingual Drug Safety Coordinator to support pharmacovigilance activities. The role involves handling clinical information, liaising with clients, and ensuring accurate documentation for safety reporting.

The ideal candidate will be bilingual (English/French), have a science background, and be comfortable with multi-tasking in a regulated environment. On-site work is expected with standard daytime shifts.

Qualifications

  • Minimum science graduate with 6 months to 1 year experience in Drug Safety/Pharmacovigilance.
  • A diploma or degree with Life Sciences concentration is a strong asset.
  • Knowledge of Pharmacovigilance industry is an asset.
  • Adaptability to change and quick learner.
  • Experience in medical/pharmaceutical fields and medical terminology is an asset.
  • Bilingual English & French is mandatory.
  • Able to work any 8-hour shift between 8:00 AM–8:00 PM, if necessary.

Responsibilities

  • Receive, scan and document clinical information in compliance with SOPs.
  • Collaborate with clients to request information or clarification as needed.
  • Review patient information for accurate documentation.
  • Attach Post Infusion Reports to databases for proper documentation.
  • Data entry into program databases and QM System.
  • Sort, file, and review incoming documents.

Skills

Communication skills
Interpersonal skills
Organizational skills
Attention to detail
Time management
Problem solving
Computer skills (Word, Excel, PowerPt)
Remote work readiness

Education

Science degree
Life Sciences concentration
Pharmacovigilance knowledge

Tools

Microsoft Word
Microsoft Excel
PowerPoint

Job description

Innomar Strategies in Canada seeks a Bilingual Drug Safety Coordinator to support pharmacovigilance activities. The role involves handling clinical information, liaising with clients, and ensuring accurate documentation for safety reporting.

The ideal candidate will be bilingual (English/French), have a science background, and be comfortable with multi-tasking in a regulated environment. On-site work is expected with standard daytime shifts.

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