Temporary full-time (37.5 hours/week)

This position is temporary until March 2027.

- Identification and recruitment of study subjects including informed consent, randomization and implementation of study protocol (including follow-up visits with study participants)
- Maintain screening logs/records.
- Completion of Case Report Forms (CRFs).
- Serious adverse event management and reporting
- Manage all aspects of clinical trial start-up (contracts, ethics, in-hospital logistics, staff education)

Hamilton Health Sciences fosters a culture of patient and staff safety, whereby all employees are guided by our Mission, Vision, Values, and Values Based Code of Conduct. Hamilton Health Sciences is a teaching hospital and all staff and physicians are expected to support students and other learners.

To be considered for this opportunity applicants must apply during the posting period. All internal and external applicants may ONLY apply via the Careers website. This job posting is for an existing vacancy.

Hamilton Health Sciences is an equal opportunity employer and we will accommodate any needs under the Canadian Charter of Rights and Freedom, Accessibility for Ontarians with Disabilities Act and the Ontario Human Rights Code. Hiring processes will be modified to remove barriers to accommodate those with disabilities, if requested. Should any applicant require accommodation through the application processes, please contact Human Resources at (phone hidden), Ext. 46947 for assistance.

If the applicant requires a specific accommodation because of a disability during an interview, the applicant will need to advise the hiring manager when scheduling the interview and the appropriate accommodations can be made.





This competition is open to all qualified applicants, however, qualified internal applicants will be considered first. Past performance will be considered as part of the selection process. If you are a previous employee of Hamilton Health Sciences, please note: the circumstances around an employee's exit will be considered prior to an offer of employment. Proficiency in both Official Languages, French and English, is considered an asset.

If this position is temporary, selection for this position will be as per the outlined Collective Agreements:

Article 30 (k), CUPE Collective Agreement

Article 10.7 (d), ONA Collective Agreement

Article 13.01 (b) (ii), OPSEU 273 Collective Agreement

Article 14.04, OPSEU 209 Collective Agreement

Article 2.07 and Article 13, PIPSC RT Collective Agreement

Perioperative Cardiac Research Program is seeking a Jr. Research Coordinator to join our highly productive research team. The successful candidate will be assisting in the coordination of various interventional clinical trials within critical care and cardiac surgery. This role will afford an prospect to hone teamwork and leadership skills within an academic research environment. This position is for on-site work only (no remote work opportunities).

- Bachelor's degree in a relevant field of study.
- Minimum 2 years previous experience in multi-center research studies/clinical trials.
- Experience with the management of large clinical research studies and or databases.
- Basic anatomy & physiology knowledge.
- Working knowledge of ICH-GCP Guidelines and international research requirements.
- Highly efficient computer skills, extensive experience with the Microsoft office suite.

📌 Jr. Research Coordinator (Ontario)
🏢 Hamilton Health Sciences
📍 Ontario