Junior Clinical Research Associate at IQVIA supporting site management in clinical trials across Spain. Key responsibilities include site selection, monitoring visits, and regulatory compliance.
About the role
- Clinical Research Associate working on global projects in healthcare. Focused on site monitoring, recruitment plans, and protocol training with dedicated mentoring.
Responsibilities
- Performing site selection, initiation, monitoring and close-out visits, plus 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
- 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
- Access to cutting-edge in-house technology
- Dedicated mentoring
- Structured quarterly reviews on performance
- Promotion and bonus awards
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