IQVIA is seeking a Research Assistant to support clinical trial activities in compliance with all applicable regulations
Requirements
- Working knowledge of clinical trials and Good Clinical Practices (GCP)
- Familiarity with protocol-specific procedures, consent forms, and study schedules
- Proficiency in EDC entry and query resolution
- Experience in visit scheduling and regulatory binder upkeep
- Applicable certifications and licenses as required by company, state, or regulatory bodies
Responsibilities
- EDC entry and query resolution
- Maintain regulatory binder and ensure compliance with documentation standards
- Schedule and coordinate subject visits and procedures
- Assist with screening, recruiting, and enrolling research subjects
- Perform patient/research participant scheduling and collect history
- Coordinate follow-up care and laboratory procedures
- Adhere to IRB-approved protocols and assist in informed consent processes
Other
- Minimum of an associate’s degree or equivalent education and experience
- At least 1 year of experience in a clinical research setting preferred
- Strong attention to detail and ability to prioritize tasks
- Excellent communication and relationship-building skills
- This position is not eligible for sponsorship
