Clinical Research Supervisor


Clinical Research Supervisor

Laval, QC


Our client, an innovative and growing pharmaceutical company, is currently looking for a Clinical Research Coordinator to join their team in Laval. Under the supervision of the Director of Clinical Development, the incumbent of the position will oversee the monitoring activities related to clinical studies managed by CROs and assist the team in the management and development of policies and procedures required to conduct clinical studies.

Main responsibilities:

  • Supervise the monitoring activities related to clinical studies managed by CROs
  • Ensure that staff involved in the conduct of a study have the required qualifications
  • Verify standardized methods of operations closely linked the contract research organizations in the selection process or selected by the company and related to the monitoring of a clinical study
  • Ensure that research centers participating in a study are adequately managed by the selected CRO(s)
  • Conduct co-monitoring visits to research centers in the company of monitors and reviews monitoring reports issued by the CRAs
  • Communicate positive and/or negative recommendations to CROs and the company
  • Represent the company during visits to research centers or the headquarters of selected contract research organizations
  • Contribute to the writing and review of protocols, patient records, study plans and other clinical research documents
  • Collaborate in the identification and evaluation of contract research organizations
  • Identify problems that impede the completion of studies, propose solutions and collaborate in the establishment of correction mechanisms
  • Perform any other duties necessary for the proper conduct of the studies such as writing, or review of documents required for Health authorities, study reports, patient records, ICF, study protocol amendments, etc.


  • University degree in health or related field or equivalent work experience
  • Minimum of 3 years of experience as CRA
  • Knowledge in biotechnology, pharmaceutical or related field
  • Knowledge of GCPs
  • Good knowledge of the Microsoft environment software and other appropriate software
  • French an English bilingualism
  • Be willing to travel, approximately 40% of the time approximately
  • Leadership and teamworking skills
  • Priorities management, analytical and synthesis skills
  • Sense of organization and responsibility
  • Great communication skills

If you are interested in this opportunity, please send your C.V. to Celine Chabee at

Only qualified candidates will be contacted

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