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.
About the role
- Clinical Research Assistant supporting studies to improve outcomes for brain tumor patients at Duke Cancer Institute. Engaging in participant interactions and managing clinical trial operations with care and precision.
Responsibilities
- Screen and consent participants for minimal risk studies, ensuring proper documentation and ethical compliance
- Coordinate and schedule study visits, prepare necessary materials, and support participant interviews
- Collect and manage biological specimens, maintain inventory, and ensure proper handling and shipping procedures
- Enter and verify clinical data using EDC systems, run reports, and ensure data accuracy and completeness
- Collaborate and communicate with study personnel to resolve routine issues and support study implementation
- Participate actively in team meetings, committees, and continuing education opportunities
- Uphold ethical standards in research, especially when working with vulnerable populations, and ensure participant safety
Requirements
- Associate’s degree required; Bachelor’s degree preferred
- One year of relevant experience (Bachelor’s degree may substitute for experience)
- Basic Life Saving (BLS) certification from the American Heart Association or Duke-approved equivalent
- Experience in clinical research or a healthcare setting preferred
- Familiarity with Electronic Data Capture (EDC) systems and Case Report Forms (CRFs/eCRFs) preferred
- Strong written and verbal communication skills
- Ability to work independently and as part of a team
- Knowledge of ethical guidelines and regulatory requirements for clinical research
Benefits
- comprehensive and competitive medical and dental care programs
- generous retirement benefits
- wide array of family-friendly and cultural programs to eligible team members
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