Clinical Research Associate Jobs in Texas
Clinical Research Associate jobs in Texas are highly active, with strong demand across pharmaceutical, biotechnology, and medical device sectors at every level from entry-level coordinators through senior CRAs and lead monitors. Houston, Dallas, and Austin are the primary hiring centers, anchored by employers such as AstraZeneca, Abbott, and MD Anderson Cancer Center. The most in-demand specialties are oncology trials, cardiovascular studies, and Phase II to Phase IV monitoring across large academic medical centers and contract research organizations. Find a role that fits below and apply directly.
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Showing 5 of 126+ Clinical Research Associate jobs
JOB SUMMARY
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:
- Nursing
- Dietetics
- Nutrition Science
- Pharmacist
- Pharmaceutical/Device Sales Representative
- Physical and Occupational Therapists
- Biomedical/Chemical Engineer
- PhD/Post-Doc
- Pharm.D
- Health and Wellness Education Coordinators
- Public Health
- Clinical Research Coordinators
- Research Assistants
MEDPACE CRA TRAINING PROGRAM (PACE®)
No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:
- PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- PACE® will prepare you by developing your CRA skills through interactive discussions and hands-on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
WHY BECOME A CRA
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Competitive pay and many additional perks unmatched by other CROs (SEE BELOW).
WE OFFER THE FOLLOWING
- Competitive travel bonus;
- Equity/Stock Option Program;
- Training completion and retention bonus;
- Annual merit increases;
- 401K matching;
- The opportunity to work from home;
- Flexible work hours across days within a week;
- Retain airline reward miles and hotel reward points;
- Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
- In-house travel agents, reimbursement for airline club, and TSA pre-check;
- Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
- CRA training program (PACE®);
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
- In-house administrative support for all levels of CRAs; and
- Opportunities to work with an international team of CRAs.
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
- On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
QUALIFICATIONS
- Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement;
- Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required;
- Must maintain a valid driver’s license and the ability to drive to monitoring sites;
- Proficient knowledge of Microsoft® Office;
- Strong communication and presentation skills; and
- Must be detail-oriented and efficient in time management.
MEDPACE OVERVIEW
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
WHY MEDPACE?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
DALLAS PERKS
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with nonprofit organizations
- Structured career paths with opportunities for professional growth
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Free on-site parking
- Outdoor seating and workspace
AWARDS
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
JOB SUMMARY
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:
- Nursing
- Dietetics
- Nutrition Science
- Pharmacist
- Pharmaceutical/Device Sales Representative
- Physical and Occupational Therapists
- Biomedical/Chemical Engineer
- PhD/Post-Doc
- Pharm.D
- Health and Wellness Education Coordinators
- Public Health
- Clinical Research Coordinators
- Research Assistants
MEDPACE CRA TRAINING PROGRAM (PACE®)
No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:
- PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- PACE® will prepare you by developing your CRA skills through interactive discussions and hands-on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
WHY BECOME A CRA
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Competitive pay and many additional perks unmatched by other CROs (SEE BELOW).
WE OFFER THE FOLLOWING
- Competitive travel bonus;
- Equity/Stock Option Program;
- Training completion and retention bonus;
- Annual merit increases;
- 401K matching;
- The opportunity to work from home;
- Flexible work hours across days within a week;
- Retain airline reward miles and hotel reward points;
- Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
- In-house travel agents, reimbursement for airline club, and TSA pre-check;
- Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
- CRA training program (PACE®);
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
- In-house administrative support for all levels of CRAs; and
- Opportunities to work with an international team of CRAs.
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
- On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
QUALIFICATIONS
- Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement;
- Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required;
- Must maintain a valid driver’s license and the ability to drive to monitoring sites;
- Proficient knowledge of Microsoft® Office;
- Strong communication and presentation skills; and
- Must be detail-oriented and efficient in time management.
MEDPACE OVERVIEW
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
WHY MEDPACE?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
DALLAS PERKS
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with nonprofit organizations
- Structured career paths with opportunities for professional growth
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Free on-site parking
- Outdoor seating and workspace
AWARDS
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
See All 126+ Clinical Research Associate Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
Find JobsClinical Research Associate Jobs by City in Texas
Where Texas roles are concentrated, by current openings.
Clinical Research Associate Job Market in Texas
A snapshot from current Texas openings, updated as new roles post.
Who's Hiring
- Baylor College of Medicine23
- Medpace20
- Baylor Scott & White Health10
- Texas A&M AgriLife Extension7
- The University of Texas at Austin6
Top Industries Hiring
- Education70
- Healthcare & Medical Services28
- Science & Research22
- Biotechnology & Pharmaceuticals14
- Agriculture & Farming3
What Texas Employers Look For
The qualifications that appear most often in clinical research associate jobs across Texas.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Society of Clinical Research Associates or equivalent GCP certification strongly preferred
- Minimum two years of clinical trial monitoring or coordination experience in a site or sponsor setting
- Solid understanding of FDA regulations, ICH E6 guidelines, and 21 CFR Parts 11 and 312
- Willingness to travel to investigator sites across Texas and surrounding regions
- Proficiency with electronic data capture systems such as Medidata Rave, Veeva Vault, or Oracle Clinical
Clinical Research Associate Jobs in Texas: Frequently Asked Questions
How do you become a clinical research associate in Texas?
Start with a bachelor's degree in life sciences, nursing, pharmacy, or a related field, then gain hands-on clinical experience through research coordinator or data management roles at a Texas academic medical center, hospital system, or contract research organization. Texas does not issue a state-specific CRA license, but earning the Certified Clinical Research Associate credential through the Society of Clinical Research Associates significantly strengthens your candidacy with most Texas employers and CROs.
Which companies hire clinical research associates in Texas?
Employers hiring clinical research associates in Texas right now include Baylor College of Medicine, Medpace, and Baylor Scott & White Health, based on current listings on Migrate Mate as of June 2026. Texas's concentration of major medical centers, pharmaceutical manufacturers, and contract research organizations means hiring is consistent year-round rather than seasonal.
Which Texas cities have the most clinical research associate jobs?
Houston, Irving, and Dallas have the most clinical research associate openings in Texas. Houston leads because of its dense cluster of cancer centers, petroleum-adjacent biotech firms, and the Texas Medical Center, the largest medical complex in the world, while Dallas and Austin draw demand from their growing pharmaceutical headquarters and CRO regional offices.
Are there remote clinical research associate jobs in Texas?
Yes, and more than many clinical roles, since a significant portion of CRA work involves remote source data verification, document review, and sponsor-side reporting. About 5% of clinical research associate openings tied to Texas are remote or hybrid as of June 2026, reflecting an industry shift toward risk-based monitoring models. Site initiation visits and close-out visits still require in-person travel, so fully remote positions typically cover Phase I or centralized monitoring functions.
How can I get hired as a clinical research associate in Texas with little or no experience?
The most realistic entry path is a clinical research coordinator role at a Texas academic medical center such as UT Southwestern, UTHealth Houston, or Baylor Scott and White, where you manage site-level trial operations before transitioning to sponsor-side monitoring. Large CROs with Texas offices often post junior or associate CRA openings specifically designed for coordinators making that move. Earning a Good Clinical Practice certification and completing a few years as a coordinator, regulatory affairs assistant, or clinical data associate makes the transition substantially more straightforward.
Where can I find and apply to clinical research associate jobs in Texas?
You can find and apply to clinical research associate jobs in Texas on Migrate Mate, which lists current Texas openings across pharmaceutical companies, contract research organizations, and academic medical centers. Find roles that fit your experience level and apply directly to the ones that match.
See All 126+ Clinical Research Associate Jobs in Texas
Find roles in Texas that match your experience and apply in just a few clicks.
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