ZipRecruiter

Log In

1

Medpace Jobs in Texas (NOW HIRING)

Medpace, Inc.

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 ...

Medpace, Inc.

Senior Contract Specialist

Irving, TX · On-site +1

$91K/yr

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 ...

Medpace, Inc.

ServiceNow Platform Engineer

Irving, TX · Hybrid

$50.25 - $69/hr

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 ...

Medpace, Inc.

ServiceNow Platform Engineer

Irving, TX · On-site

$50.25 - $69/hr

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 ...

previous page

Showing results 41-56

All JobsMedpace JobsMedpace Jobs in Texas

Medpace information

See Texas salary details

$10

$55

$91

How much do medpace jobs pay per hour?

As of Aug 25, 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.

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.

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.

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.

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 requires candidates to meet specific qualifications, including relevant experience and education. Applicants can apply online and may need to undergo interviews and assessments as part of the hiring process.

Does Medpace offer remote work?

Medpace offers remote work options for certain roles, especially those involving data analysis, project management, and clinical research coordination. Remote positions typically require strong communication skills and familiarity with collaboration tools like Microsoft Teams or Zoom. Availability of remote work may vary by position and location.

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 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 study protocols, ensure regulatory compliance, and work with clinical data using specialized tools. The role often requires knowledge of Good Clinical Practice (GCP) and relevant certifications.

What are popular job titles related to Medpace jobs in Texas?

For Medpace jobs in Texas, the most frequently searched job titles are:

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, 96% Full Time, and 2% Part Time. Highlights an 15% Physical, 15% Hybrid, and 70% Remote job distribution, with an average salary of $116,474 per year, or $56 per hour.

R Programmer

Medpace, Inc.

Irving, TX • On-site

Other

Medical, Retirement, PTO

Posted 20 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Job description

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 identify needs and establish solutions spanning data analytics, visualization, and accessibility. Programmers will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Programmers will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering teams.
Responsibilities
  • Evaluate data needs for assigned projects and make recommendations on strategic approach specific to the study design;
  • Work alongside operational and medical leads to contribute innovative data products (primarily Shiny applications);
  • Contribute to internal R package development for efficient cross-departmental programming practices;
  • Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting;
  • Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and
  • Support departmental process improvement initiatives.

Qualifications
  • Bachelor's in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field;
  • Analytical thinker with great attention to detail;
  • Ability to prioritize multiple projects on a sprint schedule;
  • Excellent verbal communication skills;
  • Programming experience in R;
  • Work experience with clinical data;
  • Experience building web applications is preferred (with either Shiny or Streamlit); and
  • Experience building dashboards is preferred (with either PowerBI, Tableau, or Spotfire).

Additional Considerations
We are hiring all levels of experience. Degree level, work experience, interview performance, and programming proficiency will be considered. Prior to the interview stage, a programming assessment will be conducted, details will be shared with candidates during scheduling confirmation.
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.

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Medpace logo

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

View All Medpace Jobs

Apply