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Rejuvenation
Overview
Coordinate all clinical trial activities in compliance with protocols and regulatory requirements. This includes recruiting participants, conducting research visits, and maintaining accurate study documentation using the RealTime CTMS system.
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Compensation
Salary not listed
Posted
14 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.
Indero
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits to ensure clinical trials adhere to protocols and regulatory standards. They also build relationships with investigators, perform source data verification, and may mentor other CRAs while overseeing site metrics.
16 days ago
Bayshore
Administer and monitor specialized pharmacological treatments and investigational medicinal products in home, clinic, or community settings. Ensure strict adherence to clinical trial protocols, regulatory requirements, and accurate documentation of patient data.
1 month ago
Probity Medical Research Inc
The Source Worksheet Development Assistant is responsible for preparing data capture tools and performing administrative tasks for clinical trials. They must ensure regulatory compliance and maintain accurate study documentation within the company's online platform.
CA$25 - CA$25 / HOUR
The Registered Nurse delivers specialized infusion and injectable treatments in home or clinic settings while monitoring patients for adverse reactions. They are responsible for developing individualized care plans, performing health assessments, and maintaining accurate clinical documentation.
I R C M
The nurse will perform technical nursing procedures and assist with complex physiological tests for clinical research trials focused on diabetes. Responsibilities include participant recruitment, patient monitoring, biological sample processing, and ensuring regulatory and ethical compliance.
CA$63,261 - CA$63,261 / YEAR
Centricity Research
The Clinical Screening Coordinator leads research-related recruitment initiatives and screens patients for clinical study participation based on protocol criteria. They are responsible for maintaining recruitment logs, managing databases, and performing clinical tasks such as obtaining vital signs and completing source documents.
CA$40,000 - CA$50,000 / YEAR
The Registered Nurse delivers specialized infusion and injectable pharmacological treatments in home and clinic settings while monitoring patients for reactions. They are responsible for developing individualized care plans, conducting health assessments, and accurately documenting all procedures and adverse events.
The Specialty Pharma Nurse delivers specialized infusion and injectable treatments in home or clinic settings while monitoring patients for adverse reactions. They are responsible for developing individualized care plans, performing health assessments, and maintaining accurate clinical documentation.