Role and responsibilities
The successful candidate will be responsible for the following tasks:
Provide information to healthcare professionals, consumers and medical sales representatives according to the approved product labelling and internal procedures
Enter all requests for medical information and drug safety in the computerized database and generate database reports as needed
Respond to requests for information on adverse drug reactions (ADR)
Reponsible for initial adverse event case processing, i.e.collect relevant information pertaining to case reported according to the internal procedure
Be compliant with the product quality (i.e. ISO 13485 standard and regulation on medical devices)
Process and document product complaints according to the internal procedure established
Provide support for health authority safety inspections
Conduct literature searches and provide summarizes as needed
Assist in drafting product labelling (e.g. product monograph) for regulatory submissions upon request
Participate in the preparation of training modules and materials for new product launches
Contribute to the medical content and revision of promotional materials and websites
Demonstrates technical and scientific skills in the research and interpretation of scientific data
Excellent written and analytical skills
Excellent communication, documentation, organizational and interpersonal skills
Ability to adapt and be flexible
Bachelor of Science Degree
Previous medical information/drug safety experience in the pharmaceutical industry, an asset
Ability to use a computerized database (knowledge of IRMS, an asset)
Proficient Microsoft Office and internet skills
We offer a competitive salary and a full range of fringe benefits. This is a permanent position and available immediately. If you are interested and have the required qualifications, send us your resume.
We thank all applicants for their interest; however, only selected candidates will be contacted.
Duchesnay is an equal opportunity employer.