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Clinical Project Manager
Job summary
A leading recruitment agency in Ottawa is seeking a Project Manager - Clinical Research for a medical device manufacturing client. This full-time, temporary role requires a postsecondary degree and 6+ years experience in managing clinical studies. The candidate will oversee clinical trials, ensuring compliance with regulations while monitoring progress and managing cross-functional teams. Competitive benefits, including medical and dental coverage after qualification, are offered.
Benefits
Qualifications
- 6+ years experience in managing clinical studies or equivalent product development programs.
- Experience in in vitro diagnostic / medical device related studies is an asset.
- Working knowledge of new product development methodologies an asset.
Responsibilities
- Oversees and resolves operational aspects of clinical trials.
- Monitors and reports progress of clinical studies.
- Communicates and works with cross-functional teams.
Skills
Education
This is an opportunity is a 1 year contract offering full time hours, Monday – Friday. The salary for this position will be determined based on education and experience.
Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.
Ottawa, ON
Monday – Friday
Full-time | Temporary
Hires fast, pays weekly.
4% vacation pay paid out on each weekly pay cheque.
Medical and dental benefits once qualified.
Free training programs
New and quicker onboarding process
Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations.
Oversees development of clinical documents, including clinical plans, protocols, forms, and reports.
Manages team to prepare for clinical study initiation, execution and close out activities.
Monitors and reports progress of clinical studies and follows up with team members and line managers when issues develop.
Communicates and works with cross-functional teams to resolve issues that arise during clinical studies.
Ensures consistency of clinical study and processes across clinical trials.
Travels as necessary to aid in program facilitation.
Postsecondary degree or diploma in Life Sciences, Biochemistry / Chemistry, Nursing, or equivalent.
6+ years experience in managing clinical studies or equivalent product development programs.
Experience in in vitro diagnostic / medical device related studies is an asset.
Knowledge of Good Clinical Practice and regulations governing in vitro diagnostics / medical devices is desirable.
Advanced skills in project planning and management, judgment, decision making, and problem solving.
Working knowledge of new product development methodologies an asset.
Ability to be creative in achieving objectives while ensuring compliance to regulatory requirements.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.