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Thermo Fisher Scientific
Overview
Coordinates and oversees clinical trial activities, including drafting and negotiating budgets and contractual terms with study sites. Manages administrative tasks such as eTMF reviews, site documentation, and ensuring compliance with regulatory guidelines and SOPs.
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Compensation
Salary not listed
Posted
3 days ago
The Memory Clinic
The Clinical Trial Associate manages regulatory tasks for Alzheimer's research trials, including IRB submissions and the maintenance of master files. They coordinate start-up activities and ensure ongoing compliance with ICH-GCP regulations and sponsor requirements.
CA$60,000 - CA$90,000 / YEAR
4 days ago
Rejuvenation
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.
17 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.
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
Provincial Health Services Authority (PHSA)
Clinical practice in radiation oncology. Research in brachytherapy, SABR, SRS, and adaptive radiotherapy. Participation in clinical trial development. Training in at least two brachytherapy techniques
Everest Clinical Research
The Clinical Trial Assistant will interact with sponsors, sites, and vendors to ensure timely and high-quality operationalization of clinical trials while compiling and reviewing documentation for site qualification and regulatory submissions. Responsibilities also include setting up, maintaining, and archiving essential documents in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
CA$45,000 - CA$65,000 / YEAR
2 months ago
