The Research Project Coordinator I will coordinate logistics, review requirements, and confirm accuracy for the shipping and collection of materials and supplies for the main study as well as for sub-studies. Assist with Troubleshooting and problem-solving issues with study systems, reports, data queries.

Support Research Project

Coordinator II-III and Research Project Manager I-III to oversee the management and reporting of data (e.g., creating/testing data reports, assisting with database set-up, validating data). Request and review reports from the Statistics and/or ICT Department(s) to maintain data integrity of the study. Develop and maintain study support tools, reports, and trackers (i.e. manuals, instructional documents). Maintain and manage access to study database and systems for all study personnel. Maintain ongoing communication with sites regarding all study related materials and issues to ensure all materials are up to date. Compile and review documentation required for Positive Clinical Practice and/or as required from the study sponsor. Coordinate drug supply and demand with study sponsor and IP manufacturer, packager, distributor to prevent shortages and overages. Perform activities related to major protocol deviations and data transfers. Provide training to PHRI and external study staff. Implement protocol amendments in consultation with the Research Project Coordinator II-III/Research Project Manager I-III/(Associate) Program Manager, Research Operations. Review IP-related information provided on study CRFs. Apply and resolve queries. Provide user access to IP management systems (IVRS/IWRS). Other duties as assigned.

1.Bachelor’s degree related to Health or Business preferred.





2.Proficient in Microsoft Office Suite.

3.Ability to problem-solve, work independently, adapt to constant change, take initiative, self- motivate, be flexible, and multi-task.

4.Excellent communication (written and verbal) and interpersonal skills.

5.Familiarity with electronic data capture software and data authoring software such as Framemaker, iDataFax, TrialMaster, or RedCAP.

Monday-Friday; 37.5 hours weekly

This position is temporary until September 2027.

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 The Population Health Research Institute (PHRI), a joint institute of Hamilton Health Sciences and McMaster University, with over 300 employees working directly with 60 researchers. PHRI conducts clinical research internationally in 105 countries and is a world leader in large, global health and population and health outcomes research. Our capacity to conduct multiple international studies concurrently, with tens of thousands of participants in each, is a capability very few organizations in the world can match.

📌 Research Project Coordinator I (Ontario)
🏢 Hamilton Health Sciences
📍 Ontario