Experienced Clinical Research Associate (CRA II/Senior/Principal) - Montreal, QC

Thermo Fisher Scientific
Canada
CAD 60,000 - 80,000
Job description

Employer Industry: Life Sciences and Clinical Research


Why consider this job opportunity:

  1. Competitive remuneration and annual incentive plan bonus
  2. Opportunity for career advancement and growth within the organization
  3. Work in an innovative and forward-thinking environment
  4. Comprehensive healthcare and employee benefits
  5. Chance to make a positive impact on global health through clinical research
  6. Supportive company culture focused on integrity, intensity, involvement, and innovation

What to Expect (Job Responsibilities):

  1. Monitor investigator sites using a risk-based approach, applying critical thinking and problem-solving skills to ensure compliance
  2. Conduct remote and on-site visits to verify protocol adherence and manage documentation
  3. Escalate deficiencies and issues to clinical management and follow through to resolution
  4. Maintain regular communication with investigative sites to ensure timely data recording and issue resolution
  5. Provide trial status updates to the Clinical Team Manager as required and ensure compliance with relevant regulations

What is Required (Qualifications):

  1. Bachelor's degree in a life science related field or equivalent Registered Nursing certification
  2. Previous experience as a clinical research monitor: 1+ years for CRA (Level II), 2+ years for Sr CRA (Level I), 3+ years for Sr CRA (Level II), and 5+ years for Principal CRA
  3. Valid driver's license where applicable
  4. Proven clinical monitoring skills and understanding of medical terminology
  5. Ability to maintain knowledge of ICH GCPs and applicable regulations

How to Stand Out (Preferred Qualifications):

  1. Experience in risk-based monitoring concepts and processes
  2. Strong oral and written communication skills, particularly with medical personnel
  3. Proven ability to manage multiple projects and work effectively under pressure
  4. Experience with Microsoft Office and other relevant software
  5. Demonstrated ability to work independently and as part of a team
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