Clinical Research Coordinator

Clinical Research Coordinator

Location: Newmarket


Responsibilities :

Monitors activities conducted by clinical investigative sites as they relate to clinical studies to ensure successful execution of the protocol.

Ensures adherence to regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.

Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

Requirements :

Bachelor’s Degree required; Medical/Science/Nursing.

Strong communicator; English must be at advanced level, oral and written.

Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in clinical research monitoring.

Experience in Healthcare a great asset.

Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.

Ability to work, understand and follow work processes within the assigned function.

Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated.


Please send resumes to :


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