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CAMH
Overview
The Coordinator integrates the voices of people with lived experience and family members into the planning, operations, and evaluation of research activities at CAMH. Key duties include facilitating patient-research partnerships, supporting the recruitment of patient advisors, and ensuring compliance with research ethics board requirements.
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Compensation
CA$38 - CA$51 / HOUR
Posted
8 days ago
Fortrea
The role involves managing all aspects of clinical site monitoring, including initiation, routine visits, and close-out for oncology trials. Key duties include ensuring patient safety, verifying informed consent, and maintaining data integrity through CRF review and SAE reporting.
Salary not listed
9 days ago
Providence Healthcare
The Interviewer recruits and prescreens participants and conducts structured interviews for various research studies. They are also responsible for data collection, data entry, and performing community outreach to connect participants with services.
CA$23 - CA$29 / HOUR
11 days ago
University of Guelph
The role involves a balance of hands-on patient care, including screening candidates and assisting in surgical procedures, and administrative coordination of clinical trials. Responsibilities include managing study logistics, collecting clinical data, and coordinating with external veterinary clinics.
14 days ago
Worldwide Clinical Trials
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Centricity Research
The coordinator will manage clinical study visits, ensure participant safety, and handle recruitment and enrollment processes. They are also responsible for maintaining accurate study documentation and ensuring compliance with regulatory requirements and protocols.
17 days ago
Winnipeg Regional Health Authority
The Research Nurse screens potential patients for clinical trial eligibility, manages consent processes, organizes treatment plans, and monitors the progress of enrolled adult and/or pediatric patients in clinical trials. They also review new studies for nursing feasibility and participate in patient/family education and specimen coordination.
CA$42 - CA$51 / HOUR
19 days ago
Care Access
The Clinical Research Coordinator, RN conducts delegated clinical tasks and monitoring of research participants while ensuring strict adherence to Good Clinical Practices (GCP) and protocol compliance. Key duties involve patient coordination, obtaining informed consent, performing clinical procedures like blood draws and ECGs, and managing investigational products.
20 days ago
ICON plc
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
21 days ago
Coordinate clinical studies by performing administrative and clinical tasks, ensuring participant safety and protocol compliance. Manage recruitment, screening, and data integrity while supporting monitoring visits and regulatory audits.
Support the execution of clinical research studies by recruiting participants and conducting study visits. Perform laboratory procedures including sample collection, processing, and shipping in compliance with protocols and SOPs.
28 days ago
Fraser Health
The LPN provides direct nursing care and administers Transcranial Magnetic Stimulation (TMS) treatment for clients with treatment-resistant depression. Responsibilities include performing psychosocial screenings, monitoring patient responses, and coordinating care with an interdisciplinary team.
CA$33 - CA$45 / HOUR
1 month ago
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management. Ensures the protection of study patients and the integrity of data submitted on Case Report Forms.
The Clinical Research Coordinator will support study execution by performing clinical procedures, managing participant safety, and ensuring compliance with protocols and regulatory requirements. They will also handle recruitment, screening, and data documentation to maintain high standards of study integrity.
Texas Health Resources
Performs age-appropriate patient assessments, establishes plans of care, and executes therapeutic interventions to achieve functional goals. Collaborates with the care team to manage patient progress, documentation, and discharge planning in an acute inpatient setting.
Planned Parenthood Los Angeles
This intermediate-level Medical Assistant performs all front and back office functions supporting reproductive health care delivery, including patient testing, screening, and non-judgmental education on options. Duties also encompass general back office tasks like obtaining medical history, assisting with procedures, quality control, and front office tasks such as scheduling and processing payments.
CA$25 - CA$25 / HOUR
3 months ago
Schroeder Ambulatory Centre
The MRI Technologist performs magnetic resonance imaging procedures using in-depth knowledge of anatomy, physiology, and protocols to produce high-quality diagnostic images. Key duties include patient preparation, operating and maintaining MRI equipment, monitoring patients, administering contrast media, and ensuring adherence to all safety and regulatory standards.
CA$48 - CA$56 / HOUR
