Clinical Study Manager I: Lead Trials & Compliance

Paycom - ATS; Tomball (TX); On-site; USD 85,000 - 120,000; Full time

Job summary

Paycom - ATS is seeking a Study Manager I to oversee quality research at assigned investigative sites, ensure enrollment meets sponsor expectations, and comply with FDA/ICH-GCP guidelines. You will train site staff and maintain study documentation to drive data quality and timely reporting.

Responsibilities include ALCOA-C compliance, adverse event reporting, cross-functional coordination, and guiding the study from initiation to closeout while meeting sponsor and company goals.

Qualifications

• Bachelor's degree preferred; regulatory and clinical research background valued.
• ACRP or equivalent certification is preferred.
• Minimum of 5 years experience in Clinical Research; supervisory experience preferred.

Responsibilities

• Train site teams and support conduct of subject visits per protocol.
• Ensure ALCOA-C standards for trial documentation and integrity.
• Manage adverse events reporting and safety information per guidelines.
• Monitor data quality, subject retention, and timely data reporting.
• Coordinate with cross-functional teams to ensure study readiness.

Skills

Attention to detail

Goal oriented

Strong communication

Customer service

Bilingual English/Spanish preferred

Education

Bachelor's degree preferred

High School Diploma or equivalent required

Job description

Paycom - ATS is seeking a Study Manager I to oversee quality research at assigned investigative sites, ensure enrollment meets sponsor expectations, and comply with FDA/ICH-GCP guidelines. You will train site staff and maintain study documentation to drive data quality and timely reporting.

Responsibilities include ALCOA-C compliance, adverse event reporting, cross-functional coordination, and guiding the study from initiation to closeout while meeting sponsor and company goals.