Research Associate contributing to NIH - funded studies in Dr. Christina Dyar's lab. Managing operations and participant communications, while contributing to manuscripts and presentations.
About the role
- As a Clinical Research Associate at IQVIA, you will monitor clinical sites and ensure compliance with GCP and ICH guidelines. Responsible for site management and recruitment planning in Poland.
Responsibilities
- Perform monitoring and site management work for clinical trials.
- Conduct site selection, initiation, monitoring, and close-out visits.
- Support the development of subject recruitment plans.
- Establish communication and administer training to assigned sites.
- Evaluate quality and integrity of site practices and escalate issues as needed.
- Track regulatory submissions, recruitment, CRF completion, and data query resolution.
Requirements
- Minimum of a Bachelors Degree in scientific discipline or health care.
- Experience of 1 year in on-site monitoring clinical trials.
- Good knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines).
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
- Good command of Polish and English language.
Benefits
- Health insurance
- Bonuses
- Professional development opportunities
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