Senior Clinical Research Coordinator - Site Lead

Dm Clinical Research Group; Irving (TX); On-site; USD 70,000 - 110,000; Full time

Job summary

Paycom - ATS seeks an experienced Clinical Research Coordinator (CRC III) to ensure quality research at assigned investigative sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. You will oversee patient visits, data entry, and site training across multiple studies.

You will liaise with Laboratory, Data, Administrative staff, and investigators to support enrollment, follow-up, and timely reporting of study activities, while maintaining ALCOA-C documentation and

Qualifications

• Minimum of 5 years experience in Clinical Research.
• Supervisory experience preferred.
• Strong written and verbal communication skills in English.
• Bi-lingual English/Spanish is preferred.

Responsibilities

• Conduct patient consent discussions and ensure understanding of procedures, risks, benefits, and alternatives.
• Provide clear explanations of study protocols and ensure patients' comprehension before consent.
• Facilitate effective communication between patients, physicians, and research staff.
• Oversee reporting of Adverse and Serious Adverse Events per guidelines and sponsor requirements.
• Maintain study documents, training, and compliance with ALCOA-C standards.

Skills

Clinical Research experience

Supervisory experience

Communication skills

English proficiency

Bilingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree

Foreign Medical Graduates

Job description

Paycom - ATS seeks an experienced Clinical Research Coordinator (CRC III) to ensure quality research at assigned investigative sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. You will oversee patient visits, data entry, and site training across multiple studies.

You will liaise with Laboratory, Data, Administrative staff, and investigators to support enrollment, follow-up, and timely reporting of study activities, while maintaining ALCOA-C documentation and