Senior Clinical Research Coordinator - Study Oversight & Enrollment

Dm Clinical Research Group; Dallas, Irving (TX, TX); On-site; USD 75,000 - 110,000; Full time

Job summary

Paycom - ATS in Dallas, TX area seeks a CRC III to ensure quality research at assigned sites in line with sponsor protocol, FDA regulations, and ICH-GCP guidelines, aiming to meet enrollment targets and sponsor expectations.

Responsibilities include training, site visits, ALCOA-C documentation, data entry, adverse event reporting, and collaboration with lab, data, and clinical teams to support study protocols.

Qualifications

• Minimum of 5 years experience in Clinical Research.
• Supervisory experience preferred.
• Wide therapeutic range of clinical trials experience preferred.
• Regulatory research experience is a plus.
• ACRP or equivalent certification is preferred.
• High School Diploma or equivalent required; Bachelor's degree preferred.

Responsibilities

• Complete all required training (ICH-GCP, IATA) timely.
• Conduct and oversee study visits and protocol-required procedures.
• Maintain ALCOA-C standards in documentation.
• Data entry and query resolution per guidelines.
• Train and mentor site staff as needed.
• Oversee reporting of Adverse Events to authorities per guidelines.
• Support sponsor enrollment goals at assigned sites.
• Attend Investigator Meetings as required.

Skills

Detail-oriented

Proactive

Strong written & verbal communication

Customer service

Bilingual English/Spanish

Education

High School Diploma

Bachelor’s degree

Foreign Medical Graduates

Job description

Paycom - ATS in Dallas, TX area seeks a CRC III to ensure quality research at assigned sites in line with sponsor protocol, FDA regulations, and ICH-GCP guidelines, aiming to meet enrollment targets and sponsor expectations.

Responsibilities include training, site visits, ALCOA-C documentation, data entry, adverse event reporting, and collaboration with lab, data, and clinical teams to support study protocols.