Were looking for an experienced Research Coordinator (RC) to join our growing team. The RC plays an integral role in the Oncology Research Department. This is an exciting and challenging position conducting multicentre centred randomized clinical trials. This position requires the ability to adhere to research protocol and work with the Investigator and other team members to carry out various aspects of conducting a clinical trial.
The Oncology Research Coordinator reports to the Manager of Research Oncology with accountability to the Oncology leadership team.
- Patient screening recruitment and consenting according to the study protocol
- Assist Investigators in the initiation of new research
- Ensure completion of eligibility requirements prior to enrollment and randomization
- Facilitate and coordinate the planned cancer treatment schedule for each trial patient
- Carrying out all study procedures including patient assessments coordinating laboratory pharmacy and diagnostic activities pertaining to study
- Specimen preparation and shipping to external labs as per IATA regulations
- Scheduling patient appointments liaising with various hospitals and health service facilities
- Adherence to all appropriate regulations in the conduct of research
- Accurate data collection transcription and entry; timely reporting of Adverse Events and Serious Adverse Events to study sponsor physician and appropriate authorities; resolving sponsor queries
- Maintenance of source documentation and ensuring that copies of test reports progress notes toxicity assessments etc. are available in patient medical charts
- Interact with sponsoring agencies regarding requests for clarifications of data and / or assisting monitors during site visits
- Participate in educational programs workshops and seminars to broaden knowledge update and develop new skills
- Represent the William Osler Oncology Department at protocol development study initiation and investigator meetings
Qualifications :
Bachelors Degree in health science or related fieldMinimum two years experience as a Research CoordinatorAdvanced knowledge of Tri-Council Policy Statement : Ethical Conduct for Research Involving Humans and Health Canadas Part C Division 5 of the Food and Drug RegulationsCertification as a Clinical Research Associate (SOCRA / ARP) or in the process of completionKnowledge of Microsoft software applications (Word Excel PowerPoint) as well as electronic data entry (EDC) softwareKnowledge of anatomy physiology pharmacology laboratory and diagnostic testingPrevious experience in Oncology is an assetFlexible and cooperative spirit with a strong commitment to team effortsProven ability to prioritize workload and meet deadlinesOutcome-drive self-starter with the ability to work independentlyExcellent organizational prioritization and time-management skillsExceptional problem-solving and decision-making skillsAdditional Information :
Hours : Currently days 8 hours (subject to change in accordance with operational requirements)
Annual Salary : Minimum : $79521.00
Maximum : $99391.00
Fully Onsite : Roles involved in direct patient care that are needed onsite for each shift.
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Application deadline : December 24 2025
Osler values inclusivity and diversity in the workplace. We welcome and encourage applicants from diverse backgrounds. We are committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act. If you require an accommodation at any stage of the recruitment process please notify Human Resources at .
While we thank all applicants only those selected for an interview will be contacted. Any information obtained during the course of recruitment will be used for employment recruitment purposes only and not for any other purpose.
Remote Work : No
Employment Type : Contract
Key Skills
Hospital Experience,Acute Care,Basic Life Support,ICU Experience,Infusion Experience,Triage,TFS,Conflict Management,Nursing,Critical Care Experience,Epic,Medication Administration
Experience : years
Vacancy : 1