Clinical Research Professional

Description:

The Research Institute of the McGill University Health Centre (RI-MUHC), one of Canada’s leading biomedical and hospital research centres, is seeking a Clinical Research Coordinator to support its Delivering Healthy Babies Initiative within the Department of Obstetrics & Gynecology.

This role offers a unique opportunity to work in a world-class research environment dedicated to advancing patient-centered medicine and improving maternal and neonatal health outcomes. The incumbent will coordinate all aspects of the project — from research planning and ethics submissions to participant management and data analysis — contributing meaningfully to innovative perinatal research.

Key Responsibilities:

• Coordinate research activities for the Delivering Healthy Babies Initiative, ensuring smooth day-to-day operation of all project components.

• Organize and manage biological specimen collection and ensure proper documentation and storage.

• Prepare and submit research protocols, ethics applications, amendments, and renewals to relevant review boards.

• Conduct literature reviews and maintain awareness of the latest research developments in obstetrics and perinatal health.

• Create and update case report forms, ensuring accurate and efficient data collection.

• Recruit, consent, and manage participants, maintaining confidentiality and compliance with ethical standards.

• Perform primary data management and statistical analysis, ensuring data integrity and accuracy.

• Assist with manuscript preparation, research presentations, and dissemination of study findings.

• Liaise with research collaborators and assist in collecting and integrating data from multiple study sites.

• Obtain required certifications and training, including Good Clinical Practice (GCP), REDCap, and Tri-Council Research Ethics.

• Perform other related coordination duties as assigned.

Qualifications and Skills Required:

• Education:

  • Diploma of College Studies (DEC) in Health Sciences or related field.

  • Bachelor’s or Master’s degree in a health or research discipline considered a strong asset.

• Experience:

  • Demonstrated experience in clinical or academic research coordination.

  • Previous exposure to perinatal, maternal, or clinical trial research preferred.

• Technical & Professional Skills:

  • Proven ability to draft research proposals, prepare scientific presentations, and manage project timelines.

  • Strong organizational and time management skills with attention to detail.

  • Ability to work independently and manage multiple priorities in a fast-paced environment.

  • Proficiency in Microsoft Office, data management tools, and familiarity with REDCap or similar platforms.

  • Excellent written and verbal communication skills in English and French (bilingualism required).

Work Conditions:

• Status: Temporary, full-time (35 hours per week)

• Work Hours: Monday to Friday, 8:30 a.m. – 4:30 p.m.

• Location: Glen Site, 1001 Boulevard Décarie, Montreal, QC

• Work Type: On-site

Benefits and Perks:

• Four (4) weeks of vacation, plus a fifth week after five years of service

• Bank of 12 paid personal/sick/family days

• 13 paid statutory holidays per year

• Modular group insurance plan (including gender affirmation coverage)

• Telemedicine services and Employee Assistance Program (EAP)

• Defined benefit pension plan (RREGOP)

• Training and professional development opportunities

• Child care centres, corporate discounts (OPUS & Perkopolis)

• Recognition program, flexible work options, and competitive parking rates

Why Join RI-MUHC:

Working at RI-MUHC means contributing to world-class research that directly improves patient care and public health. You’ll join a diverse, inclusive, and collaborative community committed to innovation, discovery, and the highest standards of research excellence.