Clinical Research Coordinator I

(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