Clinical Trials Study Manager

Paycom - ATS; Tomball (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Paycom - ATS is seeking a Study Manager I to ensure high-quality clinical research at assigned investigative sites in accordance with sponsor protocols, FDA regulations, and ICH-GCP guidelines. You will help ensure enrollment meets sponsor expectations and company goals are achieved on time.

You will complete required trainings, maintain regulatory knowledge, enforce ALCOA-C standards, and coach site teams to conduct visits and document studies accurately, supporting data quality and study

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree preferred.
• Foreign Medical Graduates preferred.
• Minimum of 5 years experience in Clinical Research.
• Supervisory experience preferred.

Responsibilities

• Ensure quality research at investigative sites per protocol, FDA regulations, and ICH/GCP.
• Maintain readiness for sponsor and CRO visits with timely follow-ups.
• Train site teams and ensure study documentation is ALCOA-C compliant.
• Oversee subject enrollment to meet sponsor expectations and timelines.
• Keep protocol, consent forms and manuals updated at all sites.
• Communicate effectively with patients, healthcare providers and staff.

Skills

Detail-oriented

Proactive

Strong written comms

Strong verbal comms

Bilingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree preferred

Foreign Medical Graduates preferred

Job description

Paycom - ATS is seeking a Study Manager I to ensure high-quality clinical research at assigned investigative sites in accordance with sponsor protocols, FDA regulations, and ICH-GCP guidelines. You will help ensure enrollment meets sponsor expectations and company goals are achieved on time.

You will complete required trainings, maintain regulatory knowledge, enforce ALCOA-C standards, and coach site teams to conduct visits and document studies accurately, supporting data quality and study