Job Summary
The Clinical Research Coordinator plays a crucial role in implementing clinical research protocols. This position involves various responsibilities including the recruitment and screening of study participants, obtaining informed consent, and overseeing the management of study-related data. Additionally, the coordinator is responsible for performing laboratory tasks, which include phlebotomy and electrocardiograms (ECG), while ensuring compliance with Good Clinical Practice (GCP) and relevant regulatory standards.
Responsibilities
- Execute clinical research protocols effectively.
- Screen candidates and procure informed consent from participants.
- Manage and maintain study data efficiently.
- Conduct laboratory tasks such as phlebotomy and ECG.
- Ensure adherence to Good Clinical Practice and relevant regulations.
Qualifications
- A minimum of 2 years of experience in a healthcare-related field.
- Associate Degree or higher is required.
- Must obtain professional certifications like CCRC or CCRP within three years of employment.
Community Health Network provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
