Clinical Research Coordinator I: Drive Quality Trials

Paycom - ATS; Tomball (TX); On-site; USD 52,000 - 66,000; Full time

Job summary

Paycom - ATS is seeking a Clinical Research Coordinator I to support investigative sites, ensuring quality data per sponsor protocol, FDA, and ICH/GCP guidelines. The CRC I will help ensure study enrollment meets sponsor expectations and timelines.

The role includes patient recruitment, consent discussions, subject visits, data entry, and collaboration with sponsor/CRO teams. Strong English communication is required; bilingual English/Spanish is preferred, and training in ALCOA-C and ICH-GCP is

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree a plus.
• ACRP or equivalent certification preferred.
• Registered Medical Assistant certification or equivalent preferred.
• 1+ year of CRC experience; 2+ years in related clinical research roles preferred.

Responsibilities

• Completing required training (ICH-GCP, IATA) before study start and ongoing.
• Conducting subject visits and protocol procedures with timely documentation.
• Maintain ALCOA-C standards in study documentation and data handling.
• Data entry and query resolution per sponsor guidelines and timelines.
• Assist in participant recruitment/retention and conduct informed consent discussions.

Skills

Communication skills

Bilingual English/Spanish

Multitasking

Education

High School Diploma

Bachelor's degree

Job description

Paycom - ATS is seeking a Clinical Research Coordinator I to support investigative sites, ensuring quality data per sponsor protocol, FDA, and ICH/GCP guidelines. The CRC I will help ensure study enrollment meets sponsor expectations and timelines.

The role includes patient recruitment, consent discussions, subject visits, data entry, and collaboration with sponsor/CRO teams. Strong English communication is required; bilingual English/Spanish is preferred, and training in ALCOA-C and ICH-GCP is