Clinical Research Coordinator I — Enrolment & Study Ops

Paycom - ATS; Tomball (TX); On-site; USD 45,000 - 65,000; Full time

Job summary

Paycom - ATS in Tomball, TX seeks a Clinical Research Coordinator I to ensure quality research at investigative sites in line with sponsor protocols, FDA regulations and ICH/GCP guidelines. You will help achieve enrollment targets and provide high-quality data to sponsors.

The role requires training in ICH-GCP, data management, and collaboration with laboratories, data teams, investigators, and participants.

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree a plus.
• Foreign Medical Graduates preferred.
• ACRP certification preferred.

Responsibilities

• Complete required ICH-GCP and IATA training on time.
• Complete protocol and manuals training prior to study start.
• Conduct study visits and document procedures promptly.
• Ensure ALCOA-C compliant documentation.
• Data entry and query resolution per guidelines.
• Coordinate with sponsors, labs, investigators, and participants.
• Assist with recruitment and consent discussions.
• Facilitate communication between patients and staff.

Skills

Clinical Research Coordinator

Data entry

GCP knowledge

Informed consent

Communication skills

Bi-lingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree preferred

Foreign Medical Graduates preferred

Tools

EDC systems

IVRS

IATA certification

ACRP certification

Laboratory procedures

Job description

Paycom - ATS in Tomball, TX seeks a Clinical Research Coordinator I to ensure quality research at investigative sites in line with sponsor protocols, FDA regulations and ICH/GCP guidelines. You will help achieve enrollment targets and provide high-quality data to sponsors.

The role requires training in ICH-GCP, data management, and collaboration with laboratories, data teams, investigators, and participants.