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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
Dalhousie University
serve as a consultant in pediatric infectious diseases. teach within Dalhousie University medical school and postgraduate training programs. develop a research program in clinical trials of vaccines. conduct independent research and collaborate with other investigators. clinical service and academic activity
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
Xenon Pharmaceuticals
Manage programming activities on project or study level, including CRO oversight. Act as a Programming SME for studies, authoring/reviewing specifications and QC. Develop and maintain data review and reporting tools. Ensure timely and quality delivery of programming activities. Create and validate SAS macros and utilities. Support statistical analysis, reporting, regulatory submissions, and publications. Develop SOPs and standard processes
$145,400 - $176,500 / 1 YEAR
2 months ago
Lead and manage clinical development studies in psychiatry. Serve as medical monitor and interact with global research sites. Contribute to clinical development plans and strategies. Provide scientific leadership for trial designs. Review scientific literature and develop product knowledge. Maintain awareness of external research and regulatory environments. Build relationships with Key Opinion Leaders. Draft and review regulatory submissions and scientific publications. Interpret clinical trial data and provide clinical relevance insights. Support in-licensing and out-licensing activities. Present proposals to senior management. Develop departmental goals and manage budgets. Collaborate with external vendors and stakeholders. Lead and develop team members (if any)
$344,000 - $380,400 / 1 YEAR
3 months ago
