Clinical Trial Coordinator

3 days ago

Toronto, Ontario, Canada Pharma Medica Research Inc. Full time
Job Summary

We are seeking a highly skilled and experienced Clinical Trial Coordinator to join our team at Pharma Medica Research Inc.

The ideal candidate will have a strong background in medical research, excellent communication skills, and the ability to work effectively in a fast-paced environment.

About the Role

As a Clinical Trial Coordinator, you will be responsible for ensuring that potential subjects meet the protocol requirements and that a full panel is obtained for each study.

You will work closely with the Manager, Screening and/or designate to ensure the smooth conduct of clinical studies.

Key Responsibilities
  • Read, understand, and be familiar with study protocols.
  • Communicate clearly and effectively with prospective subjects and other screening staff.
  • Conduct initial interviews with prospective subjects and record their medical history.
  • Obtain consents from prospective subjects by providing a clear explanation of all consents and answering questions or concerns.
  • Perform screening procedures such as body and height measurement, blood sample collection, sample processing and storage, vital signs, ECGs, adverse event, etc., according to the study protocol and/or SOP requirements.
  • Process, store, and ship biological samples as required to conduct a clinical study.
  • Perform general clinical duties to prepare for the clinical study (i.e., tube labeling, set up bleeding stations, etc.).
  • Perform general cleaning duties (i.e., decontaminate workstations and equipment such as centrifuges and fridges).
  • Properly complete documentation of clinical activities according to GCP, SOP guidelines, and/or FDA/TPD regulations.
  • Participate regularly in PMRI training programs including GCP, SOP training, and PMRI in-house training modules.
  • Achieve 80% or greater in all PMRI training evaluations including GCP, SOP tests, and PMRI in-house training module tests.
  • Follow Joint Health and Safety rules and regulations at all times.
  • Perform any tasks required by the Group Leader/Study Coordinator deemed necessary to conduct a clinical study.
Requirements
  • Three years community college or a university degree.
  • Familiarity with medical terminology or a nursing background.
  • Completion of a recognized Phlebotomy/ECG training program is preferred.
  • One year of working experience in a medical environment (clinic).
  • One year of CRO experience or equivalent.
What We Offer
  • Competitive compensation plan ($55,000 - $65,000 per annum)
  • Opportunities for advancement and career progression
  • A generous Employee Milestones Awards Program
  • Corporate Discounts Program
  • Learning Support Programs
  • Friendly atmosphere, culture of learning

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.

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