Clinical Research Associate – Level II
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇨🇦 Canada
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Monitoring investigator sites strategically
- Analyzing root causes and implementing solutions to improve compliance and minimize risks
- Assessing investigational products through physical inventory and records review
- Ensuring data accuracy through SDR, SDV, and CRF review during on-site and remote monitoring activities
- Reporting observed deficiencies and issues to clinical management and following through to resolution
- Conducting monitoring tasks and visits according to the approved monitoring plan
- Providing trial status tracking and progress updates to the Clinical Team Manager (CTM)
Requirements
- Oncology highly preferred
- Bilingual French/English
- Located in Quebec
- 6 months -1 year of direct onsite monitoring experience highly preferred
- Bachelor's degree in a related field or equivalent experience
- Proven ability to monitor investigator sites and assess investigational product compliance
- Outstanding critical thinking and problem-solving skills
- Proficient knowledge of ICH-GCP and regulatory standards
- Excellent communication and organizational skills
- Ability to work collaboratively within a team
Benefits
- Continuous contact with investigative sites
- Effective communication between investigative sites, the client company, and the PPD project team
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
monitoringdata accuracySDRSDVCRF reviewroot cause analysiscompliance assessmentinvestigational product assessmentproblem-solvingcritical thinking
Soft skills
communicationorganizationalcollaboration