Clinical Research Jobs in Texas at MedpaceÂ
Launch your career in global clinical research with a dynamic role supporting innovative clinical trials. These Clinical Research Jobs opportunity in Dallas offers hands-on involvement in trial operations, sponsor communications, and project management activities—all while working with one of the world’s leading CROs. Ideal for professionals seeking clinical trial jobs, this position blends purpose, growth, and scientific impact.
About the Company
Medpace is a globally recognized, full-service clinical contract research organization (CRO) offering Phase I–IV clinical development services to the pharmaceutical, biotechnology, and medical device industries. Headquartered in Cincinnati, Ohio with operations in 40+ countries, Medpace is known for accelerating clinical development through scientific expertise, disciplined trial execution, and commitment to improving global patient outcomes. With steady growth and industry-leading recognition, jobs at Medpace provide meaningful career paths for professionals driven by science, innovation, and purpose.
Job Details:
- Job Title: Clinical Research Project Coordinator – Dallas
- Location: Irving (Dallas), Texas
- Department: Clinical Trial Management
- Job ID: 10643
Job Summary
Medpace, a leading CRO specializing in biotech clinical development, is seeking a full-time, office-based Project Coordinator to join the Clinical Trial Management team. This role supports critical tasks across therapeutic areas including Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease, CNS, Ophthalmology, and others.
Medpace offers a comprehensive 4–6 week training program combining virtual and hands-on learning—ideal for individuals with or without prior clinical research experience.
Responsibilities in Clinical Research Jobs
- Support day-to-day clinical trial management activities
- Work closely with the Clinical Trial Manager (CTM) to deliver recurring tasks accurately and on time
- Compile and maintain project-specific status reports
- Interact with sponsors, study sites, and internal teams
- Oversee and perform quality control of the internal regulatory filing system
- Manage study supplies and inventory
- Create and maintain project timelines
- Coordinate project meetings and prepare high-quality meeting minutes
Qualifications for Clinical Research Jobs
- Bachelor’s degree in a Life Sciences field (minimum)
- Strong computer, organizational, and time-management skills
- Prior research experience preferred
Why Medpace?
- People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
- Over 30+ years, Medpace has contributed to breakthrough treatments across hundreds of diseases, improving lives worldwide.
Dallas Perks
- Modern, eco-friendly campus with on-site fitness center
- Flexible work environment
- Competitive PTO (starting at 20+ days)
- Competitive compensation & benefits
- Company-sponsored appreciation events
- Employee wellness programs
- Local community involvement
- Structured career pathways with strong growth opportunities
- Discounts on local sports events, gyms, and attractions
- Free on-site parking
- Outdoor seating and workspaces
