Enable job alerts via email!

Clinical Research Project Manager - Temporary Part-time Occasional (Research Institute)

IR-CUSM | Institut de recherche du CUSM | #ircusm

Montreal

On-site

CAD 60,000 - 80,000

Part time

3 days ago
Be an early applicant

Job summary

A prestigious research institute in Montreal is seeking a Clinical Research Project Manager for a temporary part-time position. This role involves managing a multicenter clinical research study, ensuring compliance with regulations, and working closely with both clients and internal teams. The ideal candidate has a Bachelor's degree in Health Science, bilingual communication skills, and significant experience in clinical trial management. Competitive hourly pay based on qualifications.

Benefits

Paid sick leave
Government pension plan
Vacation proration based on salary
Compensation for statutory holidays

Qualifications

  • Minimum of 2 years in multicenter clinical trial management or national registries.
  • Preferred experience in the pharmaceutical industry with hospital environment.

Responsibilities

  • Manage multicenter clinical research study.
  • Liaison with clients and biostatisticians.
  • Oversee project timelines and recruitment activities.

Skills

Bilingual communication in French and English
Project management
Organizational skills
Interpersonal skills
Knowledge of legal regulations for clinical research

Education

Bachelor’s degree in Health Science or related field

Tools

MS Excel
PowerPoint
Job description
Clinical Research Project Manager - Temporary Part-time Occasional (Research Institute)

Be among the first 25 applicants.

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

Job Description

Position Summary: Under the supervision of the Manager, Pediatric & Adult Research, at the Centre for Innovative Medicine (CIM) as well as following established governmental guidelines and regulations, the incumbent is responsible for the management of a multicenter clinical research study.

General Duties
  • Manages site feasibility questionnaire and qualification visits,
  • Ensures start-up activities, including site initiation,
  • Customizes study material for Canada,
  • Prepares and provides site training,
  • Primary liaison to clients, ensuring questions are answered and issues are resolved,
  • Primary liaison to biostatistician to ensure analysis of research questions are appropriately addressed,
  • Oversees project timelines and patient accrual,
  • Prepares and ships study materials to sites,
  • Follows-up on recruitment activities according to study timelines,
  • Manages other study activities such as monitoring visits, data management and statistics deliverables,
  • Follows-up on regulatory activities,
  • Prepares newsletters for sites,
  • Manages payment to sites,
  • Manages the study budget,
  • Conducts and coordinates the meeting with sponsor and other stakeholders,
  • Responsible for follow-up meetings with sponsor,
  • Provides regular status report to sponsor,
  • Offers support to sites,
  • Other duties as assigned by the supervisor.
Education / Experience
  • Education: Bachelor’s degree in Health Science or a related field,
  • A minimum of 2 years in multicenter clinical trial management or national registries for clinical research,
  • Experience in the pharmaceutical industry combined with hospital environment is preferred.
Required Skills
  • Bilingual (Excellent verbal and written communication skills in French and English),
  • Working knowledge of project and budget management,
  • Clinical research accreditation is preferred,
  • Excellent organizational skills,
  • Ability to manage multiple priorities, and prioritizing for time-sensitive issues,
  • Excellent knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP),
  • Self-directed and organized. Able to work both independently and as part of a team,
  • Excellent interpersonal skills,
  • Basic knowledge of biostatistics and Data management is preferred,
  • Proficient with technology systems (EDC, MS Excel, Power Point, etc.).
Additional Information

Status: Temporary Occasional (1-3 days per week - Flexible)

Pay Scale: $30.60 - $56.82/hour. Commensurate with education & work experience.

Work Shift: from 8:30am to 4:30pm

Work Site: GLEN Site, 1001 boul. Decarie

Website of the organization: https://rimuhc.ca/en

Please make sure to include a cover letter and your resume in one document.

Why work with us?
  • 3 days of paid sick leave per year, which includes a maximum of 1 personal day,
  • RREGOP government pension plan (defined benefit plan),
  • Vacation is prorated, based on a percentage of your salary,
  • 5.3% of your gross earnings will be added to your paycheque in lieu of statutory holidays.

To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits

THIS IS NOT A HOSPITAL POSITION.

Equal Opportunity Employment Program

The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity, diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact research.talent@muhc.mcgill.ca.

Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact research.talent@muhc.mcgill.ca.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.