Multi-Site Clinical Trials Program Manager

Epic Medical Research, LLC.; DeSoto (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

Epic Medical Research, LLC. seeks a Clinical Research Project Manager to oversee startup, enrollment, timelines, and closeout across multiple sites in Texas and nationwide. You will coordinate with investigators, sponsors, and CROs to ensure protocol compliance and study performance.

Ideal candidates have a life sciences degree and 3+ years in clinical research, with strong ICH-GCP knowledge, FDA requirements, and leadership. This role offers a mission-driven environment and meaningful work.

Qualifications

• ICH-GCP knowledge and FDA requirements for clinical research.
• Experience in coordinating multi-site clinical studies.
• Strong organizational, leadership and communication abilities.

Responsibilities

• Oversee study startup, enrollment, timelines and closeout across research sites.
• Coordinate with investigators, site teams, sponsors, and CROs.
• Track study performance, budgets and deliverables.
• Resolve operational issues and support protocol compliance and audit readiness.

Skills

ICH-GCP knowledge

FDA requirements

Clinical trial operations

Organizational skills

Leadership

Communication

Education

Bachelor’s degree in life sciences, healthcare, or related field

Job description

Epic Medical Research, LLC. seeks a Clinical Research Project Manager to oversee startup, enrollment, timelines, and closeout across multiple sites in Texas and nationwide. You will coordinate with investigators, sponsors, and CROs to ensure protocol compliance and study performance.

Ideal candidates have a life sciences degree and 3+ years in clinical research, with strong ICH-GCP knowledge, FDA requirements, and leadership. This role offers a mission-driven environment and meaningful work.