Description
We are seeking a Clinical Research Coordinator (CRC) to join our team in Brownsville, TX, and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
- Perform various clinical procedures, including ECGs, sample collection, and vital signs assessments.
- Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
- Conduct patient study visits and support participants throughout the research process.
- Prepare study materials, set up equipment, and plan logistical activities.
- Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria.
- Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
- Assist with EDC query management and resolution.
- Collaborate with investigators, sponsors, and study monitors to address study-related issues.
- Act as a patient advocate and maintain a safe environment.
Qualifications
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience conducting patient study visits and participant-facing clinical research activities.
- Demonstrated ability to recruit and screen patients according to study eligibility criteria.
- Proficiency with EDC systems.
- Strong attention to detail and ability to establish effective working relationships.
The potential base pay range for this role is $35.00-$42.00 per hour.