Job Overview
We are seeking a dedicated and detail-oriented Clinical Research Assistant to join our dynamic research team. In this role, you will play a vital part in supporting clinical trials and research projects focused on advancing medical knowledge and patient care.
Responsibilities
- Entering patient data into Electronic Data Capture systems designed for specific clinical trials
- Extrapolate data from source records into case report forms for patient procedures and visits
- Ensure timely data submission in accordance with policies and procedures.
- Shipping biological samples to core laboratories per study protocols.
- Maintain meticulous records and compliance documentation in line with FDA regulations and ICH GCP standards
- Scheduling clinical trial patients for follow up visits or diagnostics
- Ensure safety protocols are followed diligently, including proper handling of biological samples and adherence to HIPAA privacy regulations
- Administrative duties as assigned
Skills
- Detail oriented
- Excellent organizational skills
- Strong communication and interpersonal skills
- Knowledge of FDA regulations, HIPAA compliance, and ICH GCP certification for clinical trial conduct
- Excellent documentation review skills ensuring accuracy and regulatory compliance in all reports and logs
Job Type: Full-time
Pay: $15.00 - $20.00 per hour
Expected hours: 40 per week
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
