(Onsite in DeSoto, TX)
Our client is a rapidly growing clinical trial site network focused on advancing life-changing therapies through high-quality research, patient safety, and diverse enrollment.
The organization specializes in late-phase, industry-sponsored psychiatric and neurological trials across inpatient and outpatient settings.
The Clinical Research Coordinator I role in DeSoto/Dallas, TX is ideal for an early-career coordinator with some clinical research experience who wants to build hands-on skills in study execution, patient-facing research activities, and clinical trial operations under the guidance of senior team members.
Key Responsibilities
- Coordinate low- to moderate-complexity clinical trials, including scheduling, visit execution, and day-to-day operations
- Support high-enrolling screening trials as a secondary coordinator
- Conduct participant visits per protocol, including medical history collection, vitals, ECGs, phlebotomy, and specimen processing (as trained)
- Prepare and maintain study documentation, source documents, CRFs, and visit materials
- Ensure accurate documentation and maintain regulatory files and study trackers
- Support investigational product accountability under supervision
- Communicate with participants to maintain engagement and protocol compliance
- Assist with sponsor communication and monitoring visit preparation
- Support data entry, query resolution, and study metrics tracking
- Assist with screening and enrollment activities
- Prepare internal study reports under guidance from senior staff
Qualifications
- Bachelor’s degree required
- At least 6 months of clinical research experience required
- Experience with industry-sponsored clinical trials preferred
- Strong organizational and multitasking skills
- Ability to work in a fast-paced clinical research environment
- Interest in developing hands-on clinical and operational research skills