Clinical Research Project 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

Company Description

Epic Medical Research partners with sponsors to accelerate the development and delivery of new therapies through rigorous science and data-driven solutions. The organization operates clinical trial sites across Alabama, Arizona, California, Florida, Louisiana, Oklahoma, and Texas, including a site in DeSoto, TX. Its multidisciplinary team uses advanced methodologies and analytics to examine social, cultural, and biological factors that influence health, generating robust data to support effective treatment development. As a trusted contributor to healthcare innovation, Epic Medical Research focuses on high-quality research that improves health outcomes for diverse communities nationwide. Team members join a mission-driven environment committed to advancing discovery and bringing better treatments to market.

Qualifications

• Bachelor’s degree in life sciences, healthcare, or a related field.
• 3+ years of clinical research experience; project or multi-site management preferred.
• Strong knowledge of ICH-GCP, FDA requirements, and clinical trial operations.
• Excellent organizational, communication, and leadership skills.

Key Duties

• 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.