Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Dallas,TX . ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Dallas,TX . ...
Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm ...
Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm ...
R Programmer
Irving, TX · On-site +1
Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our programmers work directly with Clinical Operation teams to ...
R Programmer
Irving, TX · On-site +1
Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our programmers work directly with Clinical Operation teams to ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical ...
Clinical Informatics Analyst
Irving, TX · On-site
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 ...
Clinical Informatics Analyst
Irving, TX · On-site
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 ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project ...
Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project ...
Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm ...
Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research for a full-time, office ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research for a full-time, office ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Study Start-Up Project Manager
Irving, TX · On-site +1
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.
Study Start-Up Project Manager
Irving, TX · On-site +1
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.
Associate Clinical Trial Manager - PhD - Immunology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
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 - PhD - Immunology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
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 ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Ophthalmology to join our Clinical Trial ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Ophthalmology to join our Clinical Trial ...
Shiny App Developer
Irving, TX · On-site
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 ...
Shiny App Developer
Irving, TX · On-site
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 ...
R Programmer
Irving, TX · On-site
Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our programmers work directly with Clinical Operation teams to ...
R Programmer
Irving, TX · On-site
Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our programmers work directly with Clinical Operation teams to ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Dallas, TX · On-site +1
$33.25 - $45.25/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX
Dallas, TX · On-site +1
$33.25 - $45.25/hr
Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM ...
SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM ...
Medpace information
See Texas salary details
$10.30 - $17.67
0% of jobs
$17.67 - $25.04
0% of jobs
$25.04 - $32.41
1% of jobs
$32.41 - $39.78
11% of jobs
$45 is the 25th percentile. Wages below this are outliers.
$39.78 - $47.15
19% of jobs
$47.15 - $54.52
19% of jobs
The median wage is $54.70 / hr.
$54.52 - $61.89
22% of jobs
$63.15 is the 75th percentile. Wages above this are outliers.
$61.89 - $69.26
20% of jobs
$69.26 - $76.63
4% of jobs
$76.63 - $84
4% of jobs
$84 - $91.37
0% of jobs
$10
$55
$91
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Full-time
Medical, Retirement, PTO
Re-posted 9 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
16th of 75 rated research
Job description
Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Dallas,TX. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Responsible for management of study vendor
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
- Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred
- Experience in Phases 1-4; Phases 2-3 preferred
- 3-5 years as a project/clinical trial manager within a CRO;
- Management of overall project timeline
- Strong leadership skills
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
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- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- 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
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- 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
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- 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.
Employment Type: OTHERAbout 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