Job Description
Employer Industry: Healthcare Innovation
Why consider this job opportunity:
Opportunity for career advancement and growth within the organization
Travel flexibility with a mix of onsite and remote monitoring visits
Work within a supportive and innovative team focused on patient outcomes
Engage directly in life‑saving clinical research and contribute to the development of future medicines
Competitive salary and comprehensive benefits package
What to Expect (Job Responsibilities):
Serve as the primary point of contact for study sites, liaising with study teams
Identify and implement patient recruitment strategies at assigned sites
Monitor studies/sites according to Good Clinical Practice (GCP) standards and relevant SOPs
Provide site training to ensure compliance with regulations and trial‑specific procedures
Utilize and maintain clinical trial tracking systems and update electronic Trial Master Files as necessary
What is Required (Qualifications):
Bachelor of Science, R.N., or equivalent degree in Biological Sciences
Minimum 3 years of experience in onsite and offsite monitoring, preferably in the pharmaceutical industry
In-depth knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
Strong communication and influencing skills for effective site management
Ability to establish a home office and travel 30‑50% for monitoring visits
How to Stand Out (Preferred Qualifications):
Experience in analytical/risk‑based monitoring
Knowledge of multiple therapeutic areas, particularly Oncology and Early Development
Familiarity with various clinical systems and databases (e.g., CTMS, EDC, eTMF)
Strong problem‑solving and process improvement skills
Experience with mentorship in a clinical research setting
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Job Details
Posted Date:
February 21, 2026
Job Type:
Business
Location:
Canada
Company:
Johnson & Johnson
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.