Clinical Research Coordinator - Toronto, Canada - MedSleep Inc.

MedSleep Inc.

Verified Company

Toronto, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Clinical Research Coordinator required for a growing team of health professionals. This is a full-time position in Toronto.

Responsibilities:

Engage professionally with patients and deliver ethical and highquality research which strictly adheres to protocols, ICH-GCP Guidelines, SOPs, regulatory requirements, and professional standards focusing on exceptional patient service.
Pre-Screen participants and recruit eligible patients through various sources e.g. electronic medical records.
Handle study visits/ procedures and coordinate sleep studies.
Perform blood test, process, and shipment as per the protocol specific laboratory manual.
Conduct ECG, vital signs, height, weight, and BMI measurements.
Communicate with principal investigators, subinvestigators, sponsors, and stakeholders to ensure study objectives are met.
Prepare regulatory documents for REB submission and collect data.
Maintain research equipment, supplies and logs.
Hours of work are typically 95pm but depending on the study might be required to come in on evenings and weekends.

Qualifications:

Minimum 2 years CRC experience required. Phase 24 experience.
University Degree in Medicine (International Medical Graduate), Nursing, Life Sciences or Health Care.
CCRP/CCRC considered an asset with experience in Sleep Medicine.
Knowledge of ICH/GCP guidelines.
Phlebotomy Certificate will be highly an asset.
Knowledge of medical terminology.
Strong attention to detail with multiple tasking in a fact paced environment.
Excellent written and verbal communication and organizational skills.
Ability to work independently or with little supervision as part of a team.

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