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CRA (Level II)
4 months ago
Job Description
Join Thermo Fisher Scientific for impactful work that contributes to a healthier, cleaner, and safer world. Our global Clinical Operations team in the PPD clinical research services offers support for clinical trials, working on commercial and government contracts to develop efficient and high-quality clinical studies.
Discover Impactful Work:
Coordinate and perform all aspects of clinical monitoring and site management. Conduct remote or on-site visits to ensure protocol compliance and manage documentation, following sponsor guidelines. Build strong relationships with investigational sites and ensure trials are conducted ethically and accurately.
A day in the Life:
- Utilize a risk-based monitoring approach to identify and address site process failures.
- Ensure data accuracy through thorough reviews.
- Document observations and escalate issues promptly.
- Conduct monitoring tasks per plan and participate in investigator meetings.
- Complete administrative tasks and contribute to project improvements.
Keys to Success:
Education
- Bachelor's degree in a related field or relevant certification.
Experience
- Minimum 1 year of experience in clinical research monitoring.
- Valid driver's license.
Knowledge, Skills, Abilities
- Clinical monitoring skills and medical knowledge.
- Understanding of ICH GCPs and regulatory requirements.
- Strong critical thinking and communication skills.
- Ability to manage risks and work independently or in teams.
- Proficiency in Microsoft Office and English language.
Apply today
Thermo Fisher Scientific promotes a healthy work environment and is committed to diversity and inclusion.
Thermo Fisher Scientific promotes a healthy work environment and is committed to diversity and inclusion.