Clinical Study Manager I: Lead Trials & Data Quality

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

Job summary

Dm Clinical Research Group in Sugar Land, TX seeks a Study Manager I to ensure quality clinical research at assigned sites, compliant with sponsor protocols, FDA regulations and ICH-GCP guidelines, while supporting enrollment goals.

You will train site teams, enforce ALCOA-C documentation, manage safety reporting, and coordinate with cross-functional teams to achieve timely study milestones and sponsor expectations.

Qualifications

• Minimum of 5 years in Clinical Research.
• ACRP or equivalent certification preferred.
• Strong written and verbal communication skills in English.
• Proactive, detail-oriented and capable of leading site teams.

Responsibilities

• Ensure quality research at assigned sites in compliance with FDA regulations, ICH-GCP guidelines and sponsor protocols.
• Train site teams and enforce ALCOA-C standards for trial documentation.
• Maintain Investigator Site Binders and source documents; ensure timely data reporting.
• Support enrollment goals and readiness for sponsor/IRB visits; coordinate with cross-functional teams.

Skills

Clinical Research

Regulatory Knowledge

Documentation

Communication

Leadership

Quality Assurance

Education

Bachelor's degree

High School Diploma

Job description

Dm Clinical Research Group in Sugar Land, TX seeks a Study Manager I to ensure quality clinical research at assigned sites, compliant with sponsor protocols, FDA regulations and ICH-GCP guidelines, while supporting enrollment goals.

You will train site teams, enforce ALCOA-C documentation, manage safety reporting, and coordinate with cross-functional teams to achieve timely study milestones and sponsor expectations.