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About the role
Key responsibilities & impact- Performing site selection, initiation, monitoring and close-out visits
- Maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Requirements
What you’ll need- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
- 2 years of clinical research coordinator experience strongly preferred
- Alternatively, an equivalent combination of education, training and experience
Benefits
Comp & perks- Award winning and innovative work environment
- Access to cutting-edge in-house technology
- Dedicated mentoring and structured quarterly reviews on performance, promotion and bonus awards
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
site selectionmonitoringdocumentationsubject recruitment plan developmentprotocol administrationquality evaluationregulatory submissions trackingcase report form (CRF) completiondata query resolution
Soft Skills
communicationorganizational skills
Certifications
Bachelor's degreeCRA Trainee Program completion