Clinical Research Associate

Position open to Canadian citizen esident or with Canadian work permit

Montreal Health Innovations Coordinator Center

Full Time

The Montreal Health Innovations Coordinating Center (MHICC) is a full-service contract research organization targeted on multicenter and multinational clinical trials. We provide services to the academic community and to the pharmaceutical, biotechnology and medical device industries. Our main goal is to establish a partnership with our customers to ensure a successful implementation of their project while respecting the scope of work, budget, timelines and highest standards of quality.

Position Summary

The CRA is responsible for monitoring the progress of clinical studies at sites or remotely, and ensure clinical studies are conducted, recorded, and reported in accordance with the protocol, monitoring plan, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and other applicable regulatory requirements. This position interacts with investigators, study coordinators, pharmacists and other clinical personnel, Project Managers, and sponsors.

Responsibilities

• Monitor clinical studies at sites or remotely for compliance with the protocol, monitoring plan, SOPs, GCP and other applicable regulatory requirements and in accordance with the study timelines
• Ensure the rights and well-being of subjects are protected
• Perform pre-study, site initiation, monitoring and close-out activities
• Review clinical data, source documentation, case report form and site regulatory files for accuracy, completeness and compliance
• Prepare and submit monitoring reports and follow-up letters to the Project Manager per timelines; follow-up on site corrective actions until resolution
• Manage assigned sites to ensure compliance & adequate enrollment
• Serve as a resource and main point of contact for study coordinators, investigators & other staff
• Participate in training
• Provide training and inform sites of any changes in study conduct and requirements
• Communicate with the site, sponsor and Project Manager, and ensure critical observations are immediately communicated and effective resolution is obtained
• Work with data management and the site to resolve discrepancies
• Ensure appropriate reporting & follow-up for all safety information by site staff
• Proactively identify and provide input into issues that may impact recruitment timelines
• Ensure audit/inspection readiness at sites and assist with inspection preparation
• Perform administrative functions (e.g. planning/scheduling, tracking time on clinical studies, expense reports, etc.
  
  

Requirements

• Bachelor’s degree in health sciences or nursing (mandatory)
• Bilingual (French/English) - MANDATORY
• A min. of two (2) years clinical research monitoring and/or clinical study coordination
• Excellent knowledge of clinical research methodology and solid understanding of clinical studies, ICH, GCP, and other applicable regulatory requirements
• Strong leadership, project management and interpersonal skills.
• Must have strong analytical and problem-solving skills.
• Prioritize effectively
• Computer literacy and proficient in Microsoft Office including Excel
• Selected candidates must demonstrate excellent organization, communication and management skills and leadership skills
  
  

WORK CONDITIONS

• 35 hours weekly base
• May require some travel, approx. 25-35%
• Pre-approved overtime paid
• Flexible work schedule for work-family balance
• Hybrid model (working from home and office)
• 4 weeks’ vacation after one year
• 13 statutory holidays
• Defined retirement benefits
• Group insurance
• 9.6 day off sick days
  
  

The Montreal Heart Institute offers a wide range of benefits aimed at employees' health, well-being and quality of life at work, including free access to the EPIC Centre as well as various other benefits.

TO SUBMIT YOUR APPLICATION

• Please attach your cover letter and resume
  
  

The Montreal Heart Institute subscribes to an equal access program. Applications from targeted groups (women, visible minorities, ethnic minorities, Indigenous peoples, and persons with disabilities) are encouraged

Only candidates that have been selected for an interview will receive a written answer.