Clinical Research Coordinator

Clinical Research Coordinator – Diagnostic Imaging Requisition ID: 391987 Position Number: 20078914 Posting End Date: November 19, 2025 Location: Winnipeg, Shared Health – Health Sciences Centre Department / Unit: Cyclotron Job Stream: Clinical Support Union: MAHCP Anticipated Start Date: 11/24/2025 FTE: 1.00 Anticipated Shift: Days; Standby coverage as required; On call Work Arrangement: In Person Daily Hours Worked: 7.75 Annual Base Hours: 2015 Salary: $43,236 – $51,625 Position Overview Work with the Director to support clinical trials for new radiopharmaceuticals, ensuring compliance with Good Clinical Practice (GCP). Compile, organize, format, evaluate, and submit regulatory documentation for clinical trial applications (CTAs) and ongoing research. Coordinate submissions to Research Ethics Boards (REBs). Maintain regulatory documents for clinical trials, including master files and adverse event reporting. Ensure all procedures and related documents required for a trial are in place. Act as liaison between investigators, site staff, and external partners, coordinating monitoring and auditing functions and ensuring data integrity. Establish and maintain document control for SOPs, forms, worksheets, and labels. Perform administrative duties related to research and operations. Support the synthesis and properties of radiotracers for clinical and research applications. Design and synthesize radiopharmaceuticals in the research lab (small molecules, peptides, antibodies) labeled with isotopes such as 18F, 11C, 68Ga, 64Cu, and 89Zr. Develop and optimize radiolabeling protocols to improve yield, purity, and stability. Operate and maintain key research and production instruments such as HPLC, GC, TLC, and automated synthesis modules. Collaborate with clinical and basic science departments to evaluate radiopharmaceuticals in vitro and in vivo, contributing to biodistribution, imaging, and dosimetry studies. Prepare documentation for regulatory submissions, including method validation reports and batch production records. Support clinical operations, including manufacturing, quality control of radiopharmaceuticals, and equipment electronic controls. Perform production and quality control testing of radiopharmaceuticals as required. Develop Standard Operating Procedures (SOPs) for radiopharmaceutical production and quality control. Perform equipment validations to ensure smooth operations. Contribute to research and development of new radiopharmaceuticals for clinical use, including designing and validating production methods. Analyze experimental data, draw conclusions, and make recommendations based on findings. Support manuscript preparation, presentations, and submissions for scientific publications. Train students, research assistants, and technicians in radiochemistry techniques. Adhere to all safety and health regulations and safe work practices. Perform additional duties as required, not exceeding stated skills and capabilities. Experience Minimum 2 years in a clinical or research positron emission radiopharmaceuticals (PERs) laboratory. At least 2 years in a Good Manufacturing Practices (GMP) environment. Hands‑on experience in synthesis and quality control of radiopharmaceuticals. Proficiency with analytical techniques such as HPLC, GC, and TLC. Experience in research article writing and clinical research/data management software is an asset. Experience with Canadian regulatory framework (Health Canada, CNSC) is an asset. Education Bachelor of Science degree or equivalent education and experience recognized by HSC. Certification / Licensure / Registration Designation as a Nuclear Energy Worker under applicable Canadian Nuclear Safety Commission legislation. Qualifications and Skills Independent worker with minimal supervision. Excellent oral and written communication, including technical writing. Self‑motivation, analytical, prioritization, and deadline‑management skills in a fast‑paced environment. Team‑oriented collaborative working ability. Competency with Microsoft Office and document management systems. High professionalism and respectful collaboration with team members, researchers, and stakeholders. Advanced computer skills (word processing, data management, spreadsheets). Strong time management and analytical capabilities. Physical Requirements Ability to perform essential physical tasks. Exposure to radiation kept as low as reasonably achievable. This position requires a current satisfactory Criminal Records Check (including Vulnerable Sector Search), Child Abuse Registry Check, and Adult Abuse Registry Check as conditions of employment. The successful candidate will be responsible for any associated service charges. A security check is considered current if it was obtained no more than six (6) months prior to the start of employment. Shared Health values and supports employment equity and workplace diversity and encourages all qualified individuals to apply. We thank all applicants, but only those selected for an interview will be contacted. We welcome applications from people with disabilities. Accommodations are available upon request during the assessment and selection process. Manitoba healthcare employers, in partnership with the Indigenous community, are committed to increasing the representation of Indigenous People within all levels of our workforce. Indigenous applicants are encouraged to apply and to voluntarily self‑identify as being of Indigenous descent in their cover letter/application. Seniority Level Entry level Employment Type Full‑time Job Function Research, Analyst, and Information Technology Hospitals and Health Care #J-18808-Ljbffr