Senior Clinical Research Coordinator - Queens University

Reporting to the Director of Research Operations, Queen’s Health Sciences (QHS), the Senior Clinical Research Coordinator is responsible for managing and coordinating the administration of new and ongoing, multi-center, multi-modality clinical trials for the Clinical Trials Support Unit (CTSU). The incumbent will assist in managing the conduct and implementation of various clinical research trials per protocol and under the guidance of various Principal Investigator(s). Duties may include but are not limited to the identification of eligible participants, the collection and coding of clinical data including that abstracted from clinical records and from interviews with research participants, liaising with hospital personnel, and faculty and staff to coordinate activities required to ensure the protocol is followed for each trial. Establish and maintain study databases and essential documentation, will work collaboratively with participating centres and trial committees (including investigators, clinical research associates, pharmacists), industry partners, and others in an evolving international clinical trials environment. Promotes an awareness and understanding of trial design, goals and procedures and critically evaluates incoming information for accuracy, relevance and prioritization.

This position will require travel to multiple sites in Kingston, including Kingston Health Sciences Centre (Kingston General Hospital and Hotel Dieu Hospital Sites) and Providence Care Centre.

This position will require occasional work on evenings, nights, weekends.

Review full job description, responsibilities, and special skills online.

REQUIRED QUALIFICATIONS:

• Master's degree in a relevant field.
• 5-7 years of previous experience working as a clinical trial coordinator conducting clinical trials. Previous experience involving investigational drugs/devices, informed consents, and data collection in a clinical setting.
• Understanding of research design, procedures, guidelines, and standards governing clinical research (e.g., Tri¬-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS 2); ICH Good Clinical Practice E6 (R2); Part C, Division 5 of the Food and Drug Regulations; Part 4 of the Natural Health Products Regulations; Part 3 of the Medical Devices Regulations, Ontario Personal Health Information Protection Act (PHIPA 2004); U.S. Code of Federal regulations titles 21 and 45).
• Certified Clinical Research Professional (through SoCRA or ACRP or equivalent organization) an asset.
• Biohazard training, Human Blood, Tissues, and Bodily Fluids and Transportation of Dangerous Good (TDG/IATA) course is considered an asset.
• Consideration may be given to an equivalent combination of education and experience.

Please apply online at:
https://queensu.njoyn.com/cl4/xweb/xweb.asp?tbtoken=Zl1bQBtZDVB0anZ0QVRSF09OcBJdaVUudFJMW10FBnldWTUfUDEaLiUuQC4kXmBxck0YGhJWQXJjF3U%3D&chk=ZVpaShM%3D&clid=74827&Page=JobDetails&Jobid=J0525-1092&BRID=415421&lang=1.