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Medpace Jobs in Texas (NOW HIRING)

Medpace, Inc.

Study Start-Up Project Manager

Irving, TX · On-site +1

  • Medical

  • Retirement

  • PTO

Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team.

Medpace, Inc.

Shiny App Developer

Irving, TX · On-site

  • Medical

  • Retirement

  • PTO

Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our developers work directly with Clinical Operation teams to ...

Medpace, Inc.

Clinical Informatics Analyst

Irving, TX · On-site

  • Medical

  • Retirement

  • PTO

Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to ...

Medpace, Inc.

Experienced Contract Manager

Irving, TX · On-site

$82K - $110K/yr

  • Medical

  • Retirement

  • PTO

Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and ...

Medpace, Inc.

Experienced Contract Manager

Irving, TX · On-site +1

$82K - $110K/yr

  • Medical

  • Retirement

  • PTO

Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and ...

Medpace, Inc.

Senior Contract Specialist

Irving, TX · On-site +1

$91K/yr

  • Medical

  • Retirement

  • PTO

None Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical ...

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How much do medpace jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for medpace in Texas is $56.00, according to ZipRecruiter salary data. Most workers in this role earn between $45.91 and $63.37 per hour, depending on experience, location, and employer.

Does Medpace hire?

Yes, Medpace regularly hires for various roles in clinical research, project management, and scientific fields. The company often posts job openings on its careers page and accepts applications from qualified candidates with relevant experience and education.

What skills and qualifications are needed to thrive as a clinical research associate at Medpace?

To thrive as a Clinical Research Associate at Medpace, you need a solid background in life sciences or a related field, experience in clinical trials, and strong knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and possibly certifications like SOCRA or ACRP are typically required. Excellent organizational skills, attention to detail, and effective communication are crucial soft skills for managing study sites and collaborating with diverse teams. These competencies ensure the integrity of clinical trials, regulatory compliance, and successful project outcomes.

Is Medpace a good place to work?

Medpace is a global contract research organization known for its collaborative work environment and focus on clinical trial management. Employees often cite opportunities for professional growth and a structured schedule, though experiences can vary by role and location.

What challenges do clinical research associates face at Medpace, and how does the company support their professional development?

Clinical Research Associates at Medpace often encounter challenges such as managing multiple clinical trial sites, ensuring regulatory compliance, and maintaining clear communication with both site staff and internal teams. Medpace supports its CRAs through structured onboarding, ongoing training programs, and mentorship from experienced professionals. The company also encourages career growth by providing clear advancement paths and opportunities to specialize in various therapeutic areas or move into project management roles.

What exactly does Medpace do?

Medpace is a global contract research organization (CRO) that provides clinical trial management and research services for the pharmaceutical, biotech, and medical device industries. Employees in this field typically coordinate clinical studies, ensure regulatory compliance, and utilize industry-standard tools to support drug development processes.

Does Medpace offer remote work?

Medpace offers remote work options for certain roles, especially those in clinical research, data management, and regulatory affairs. Remote positions typically require strong communication skills and familiarity with collaboration tools like Microsoft Teams or Zoom. Availability of remote work can vary by position and location, so candidates should review specific job postings for details.

What is Medpace?

Medpace is a global, full-service clinical contract research organization (CRO) that provides services to the biotechnology, pharmaceutical, and medical device industries. The company specializes in the design and management of clinical trials to help bring new drugs and medical devices to market. Medpace offers a range of services, including regulatory consulting, clinical trial management, data management, and biostatistics. Their work is critical in ensuring that new therapies are safe and effective for patients.
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What job categories do people searching Medpace jobs in Texas look for? The top searched job categories for Medpace jobs in Texas are:
What cities in Texas are hiring for Medpace jobs? Cities in Texas with the most Medpace job openings:
Medpace jobs near you
Infographic showing various Medpace job openings in Texas as of August 2026, with employment types broken down into 2% Internship, 95% Full Time, 2% Part Time, and 1% Nights. Highlights an 18% Physical, 18% Hybrid, and 64% Remote job distribution, with an average salary of $116,474 per year, or $56 per hour.

Associate Clinical Trial Manager - PhD - Immunology - Dallas

Medpace, Inc.

Irving, TX • On-site

$31 - $42.50/hr

Other

Medical, Retirement, PTO

Re-posted 29 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research

Job description

Job Summary
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Immunology, Rheumatology, Allergy or Dermatology areas for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
Responsibilities
  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
  • Compile and maintain project-specific status reports within the clinical trial management system
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors
  • Provide oversight and quality control of our internal regulatory filing system
  • Provide oversight and management of study supplies
  • Create and maintain project timelines
  • Coordinate project meetings and produce quality minutes

Qualifications
  • PhD in Life Sciences
  • Expertise related to Immunology, Rheumatology, Allergy or Dermatology
  • Ability to work in a fast-paced dynamic industry within an international team
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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