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Clinical Research Coordinator (study Manager)

June 8 2017
Industries Pharmaceutical, Biotechnology
Categories Clinical research, Nursing
Montreal, QC

Your responsibilities

Specifically, the Clinical Research Coordinator, is responsible for:

  • Management of clinical research study in terms of quality, timelines, following current standards (SOPs, WI (Work Instructions) ;
  • Ensuring that patient receive all the information needed to participate in a study ;
  • Doing follow-up of patient during their visit to the clinic ;
  • Being responsible for quality control of data for source documents ;
  • Knowing, understanding and applying internal procedures ;
  • Ensuring proper training of the team, may act as trainer if needed ;
  • Effective communication with members of the clinical research team ;
  • Completing documentation (source documents, medical file and CRF (case report form) in accordance with GCP (good clinical practices) ;
  • Actively participating in patient recruiting;
  • Communication with clients: accompanying them during visits ;
  • Ensuring a high quality customer service (pharmaceutical clients and patients);
  • Finding ways to improve clinical research processes, making recommendations;
  • Performing other related task.


  • Bachelor degree of Science or DEC in nursing ;
  • Minimum of 5 years of experience as a Clinical Research Coordinator ;
  • Knowledge of good clinical practices in clinical research (GCP) ;
  • Highly organized ;
  • Autonomous ;
  • Bilingual (spoken and written) ;
  • Basic knowledge of computer office software (Excel-Word).

Thank you for your application and please note that only selected candidate will be contacted.

The masculine gender designates both sexes with no discrimination intended, and is used only to facilitate reading.

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