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 managing monitoring and site management of clinical trials in Poland. Ensuring compliance with study protocols and regulatory requirements while supporting site communication and training.
Responsibilities
- Perform monitoring and site management work to ensure that sites are conducting the study(ies)
- Responsibilities include site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication and administering protocol training to assigned sites
- Evaluating the quality and integrity of site practices
- Managing progress by tracking regulatory submissions and data query resolution
Requirements
- Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Experience in on-site monitoring of clinical trials
- Written and verbal communication skills including good command of Polish and English language
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
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