Experienced Bilingual Clinical Research Associate (cra Ii, Sr Cra, Pcra) - Montreal, Qc
Thermo Fisher Scientific UK
Montreal, QC, Canada
Fully remote
Bachelor's degree in life sciences
Valid driver's license
Risk-based monitoring approach
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials
Job Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
The role requires applying a risk-based monitoring approach to identify site process failures and implement corrective actions to ensure data reliability.
Candidates must possess strong English and French language skills to facilitate effective communication between investigative sites, clients, and the project team.
Matching Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
Skills & Requirements
Must-have
Bachelor's degree in life sciences
Valid driver's license
Risk-based monitoring approach
ICH-GCP guidelines knowledge
English and French language skills
Nice-to-have
Critical thinking and problem-solving
Collaborative relationship building
Process improvement initiatives
Root cause analysis expertise
Flexible and adaptable mindset
Key Requirements
1 year of clinical research monitor experience
Bachelor's degree in life sciences or nursing certification
Completion of PPD Drug Development Fellowship (alternative)