Clinical Research Coordinator
Epic Medical Research
About the Role
This is a full-time, on-site Clinical Research Coordinator role based in DeSoto, TX.
Key Responsibilities
- Manage the day-to-day conduct of clinical trials.
- Participant recruitment, screening, and enrollment.
- Coordination of study visits and follow-up.
- Obtain and document informed consent.
- Ensure adherence to study protocols.
- Maintain accurate source documents and case report forms.
- Support regulatory and compliance activities.
- Collaborate with investigators, sponsors, and site staff to ensure timely data collection, query resolution, and overall study quality.
- Monitor participant safety.
- Report adverse events.
- Support continuous improvement of site operations.
Requirements & Tech Stack
- Strong clinical research experience and hands-on involvement with clinical trials.
- Skills in informed consent processes and participant education regarding study requirements and risks.
- Solid understanding of study protocol implementation and research best practices.
- Experience with data collection, documentation, and adherence to regulatory and ethical standards.
- Strong organizational, time management, and attention-to-detail skills.
- Ability to manage multiple studies or tasks.
- Effective interpersonal and communication skills.
- Ability to work on-site in DeSoto, TX.
- Ability to maintain professionalism in a fast-paced clinical environment.
- Prior experience in outpatient research sites or similar clinical settings is an advantage.
Qualifications
- Bachelor’s degree in a health-related or scientific field (or equivalent experience) preferred.
- Knowledge of Good Clinical Practice (GCP), HIPAA, and FDA/ICH guidelines beneficial.