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Clinical Research Associate (Cra) - Dallas

0-2 years
Not Disclosed
10 Oct. 19, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Associate (CRA) – Dallas

📍 Location: Irving (Dallas), Texas
🏢 Department: Clinical Research Associate
🆔 Job ID: 11094
💼 Employment Type: Full-Time


Job Summary

The Clinical Research Associate (CRA) role at Medpace offers an exciting opportunity to be part of cutting-edge drug and medical device research while making a meaningful difference in patients’ lives.

This position is ideal for individuals with a medical, health, or life sciences background who want to enter the clinical research field, travel across the U.S., and work in a collaborative environment helping bring pharmaceuticals and medical devices to market.


Who Thrives in This Role

Successful CRAs come from diverse scientific and medical backgrounds, including:

  • Nursing

  • Dietetics & Nutrition Science

  • Pharmacy / Pharm.D

  • Pharmaceutical or Medical Device Sales

  • Physical & Occupational Therapy

  • Biomedical or Chemical Engineering

  • PhD / Post-Doctoral Researchers

  • Health & Wellness Coordinators

  • Public Health Professionals

  • Clinical Research Coordinators / Assistants


Medpace CRA Training Program (PACE®)

No prior clinical research experience? No problem. Medpace offers a comprehensive training program designed to develop you into a highly skilled CRA.

PACE® (Professionals Achieving CRA Excellence) includes:

  • Interactive, hands-on job-related exercises and practicums.

  • In-house and field-based training modules.

  • Departmental rotations to understand the drug/device development and approval process.

  • Ongoing professional development with continued mentorship.


Why Become a CRA

This role offers travel, growth, and purpose—empowering you to make a global impact through the improvement of medical treatments.

Key Benefits:

  • Dynamic work with varied daily responsibilities.

  • Exposure to multiple therapeutic areas.

  • Collaboration with expert regulatory and medical teams.

  • Defined promotion pathway with opportunities for mentorship and leadership.

  • Competitive salary and unmatched perks (see below).


Compensation & Benefits

  • Competitive travel bonus.

  • Equity/Stock option program.

  • Training completion & retention bonuses.

  • Annual merit-based salary increases.

  • 401(k) matching plan.

  • Work-from-home flexibility.

  • Flexible work hours within the week.

  • Retain airline and hotel reward points.

  • Home office allowance, laptop, and mobile hotspot provided.

  • In-house travel agents and reimbursement for airline clubs and TSA Pre-check.

  • Career advancement: Lead CRA, CRA Manager, Clinical Trial Manager, Training & Development Manager, etc.

  • Continuous therapeutic training from in-house physicians and regulatory experts.

  • Administrative support for all CRA levels.

  • Global collaboration with international CRA teams.


Key Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites.

  • Communicate with site staff (investigators, coordinators, and clinical teams).

  • Verify investigator qualifications, training, and resources (staff, labs, facilities, and equipment).

  • Review and verify source documents against case report forms for accuracy and compliance.

  • Identify and correct protocol deviations per SOPs, GCP, and regulations.

  • Perform on-site and remote monitoring using risk-based approaches and CTMS tools.

  • Confirm subject eligibility for study participation.

  • Review regulatory documents and ensure compliance.

  • Manage investigational product/device accountability and inventory.

  • Verify and review adverse events and concomitant medications for accurate reporting.

  • Assess recruitment and retention performance and suggest improvements.

  • Prepare monitoring reports and follow-up letters, summarizing findings and recommending corrective actions.


Qualifications

  • Education: Minimum Bachelor’s degree in a health or science-related field (Advanced degrees preferred).

  • Experience: Prior CRA or clinical research experience preferred (In-House CRA path available for beginners).

  • Travel: Ability to travel 60–70% nationwide (some remote visits possible).

  • License: Valid driver’s license and ability to drive to monitoring sites.

  • Technical Skills: Proficient in Microsoft Office Suite (Word, Excel, Outlook).

  • Soft Skills: Strong communication, organization, attention to detail, and time management.


About Medpace

Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.

Mission: To accelerate the development of safe and effective medical therapeutics through a scientific and disciplined approach.
Headquarters: Cincinnati, Ohio
Global Presence: 5,000+ employees | 40+ countries

Therapeutic Expertise:
Oncology | Cardiology | Metabolic Disease | Endocrinology | CNS | Anti-Viral | Anti-Infective


Why Join Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Dallas Campus Perks:

  • Flexible work environment

  • 20+ days of starting PTO

  • Competitive salary and benefits

  • Employee appreciation events

  • Health and wellness programs

  • Community engagement with nonprofits

  • Modern, eco-friendly campus with fitness center

  • Discounts on sports, gyms, and attractions

  • Free on-site parking

  • Outdoor seating and workspace

  • Clear, structured career advancement


Awards & Recognition

🏆 Top Workplace 2024 – The Cincinnati Enquirer
🏆 Forbes: America’s Most Successful Midsize Companies (2021–2024)
🏆 CRO Leadership Awards – Life Science Leader Magazine
(Recognized for Expertise, Quality, Capabilities, Reliability, and Compatibility)


Next Steps

A Medpace team member will review your application. If your qualifications align, you will be contacted with details for the next steps in the hiring process.

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