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Cra Pharmaceutical Jobs (NOW HIRING)

Contract CRA

Covington, KY · On-site

$90 - $100/hr

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a ... for pharmaceutical, biotech, and medical device companies. Focused on forming long-term ...

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Cra Pharmaceutical information

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$11K

$79.4K

$137.5K

How much do cra pharmaceutical jobs pay per year?

As of Aug 3, 2026, the average yearly pay for cra pharmaceutical in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What does a CRA pharmaceutical do?

A Clinical Research Associate (CRA) in the pharmaceutical sector typically monitors clinical trials to ensure compliance with protocols and regulatory requirements, reviews data quality, and visits research sites to train staff and verify proper documentation. Daily tasks often include preparing visit reports, resolving site issues, and communicating with site coordinators and project managers. The role also involves tracking patient enrollment, ensuring the safety and rights of trial participants, and facilitating clear communication between clinical teams. As a CRA, you can expect a dynamic mix of fieldwork and remote communication, with opportunities to build strong professional relationships across the research landscape.

What is a CRA pharmaceutical?

A Clinical Research Associate (CRA) in the pharmaceutical industry monitors clinical trials to ensure compliance with regulations, protocols, and ethical standards. They work with investigators, sponsors, and regulatory agencies to ensure accurate data collection and patient safety. CRAs may travel to trial sites, review documentation, and provide training on study procedures. Their role is critical in bringing new drugs and treatments to market efficiently and safely.

What are the key skills and qualifications needed for a CRA pharmaceutical?

To thrive as a Clinical Research Associate (CRA) in the pharmaceutical industry, you need a solid background in life sciences, clinical research methodologies, and Good Clinical Practice (GCP) guidelines, often supported by a relevant degree. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) software, and GCP certification are commonly required technical qualifications. Excellent organizational skills, attention to detail, and strong interpersonal communication help distinguish top performers in this field. These skills ensure trials are conducted safely, ethically, and in compliance with strict regulatory standards while facilitating effective collaboration between sites and sponsors.

More about Cra Pharmaceutical jobs
What cities are hiring for Cra Pharmaceutical jobs? Cities with the most Cra Pharmaceutical job openings:
What are the most commonly searched types of Cra Pharmaceutical jobs? The most popular types of Cra Pharmaceutical jobs are:
What states have the most Cra Pharmaceutical jobs? States with the most job openings for Cra Pharmaceutical jobs include:
Infographic showing various Cra Pharmaceutical job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 3% Part Time, and 1% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate (CRA) - Dallas

Medpace, Inc.

Houston, TX • Hybrid

Other

Medical, Retirement, PTO

Re-posted 19 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 72 rated research


Job description

Job Summary

Join our CRA Team in Dallas, Texas!

The Clinical Research Associate position offers an exciting career within clinical research! For those with medical and life science backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!

This position is office based in Dallas, Texas.

Our successful Clinical Research Associates possess various backgrounds within the medical, healthcare, and science-related fields:

  • Nursing
  • Dietetics
  • Nutrition Science
  • Pharmaceutical/Device Sales Representative
  • Physical and Occupational Therapists
  • Biomedical/Chemical Engineer
  • Public Health
  • PhD/Post-Doc
  • Pharm.D
  • Health and Wellness Education Coordinators
  • Research Assistants
  • Clinical Research Coordinators

Medpace CRA Training Program (PACE)

No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE  (Professionals Achieving CRA Excellence) Training Program includes the following:

  • A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRA
  • Interactive discussions with hands-on exercises and practicums
  • Core departmental rotations to learn various aspects of the drug/device development and approval process

Why CRA?

  • Exciting travel opportunities
  • Make a difference on a larger scale through the development of medical drugs and devices
  • Dynamic working environment with varying day-to-day responsibilities
  • Exposure to multiple therapeutic areas
  • Defined CRA promotion and growth ladder 

We Offer the Following: 

  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • 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 membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA 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 CRA
  • Opportunity to work with 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 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
  • 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
  • Minimum of a Bachelor's degree in a health or science related field
  • Ability to travel 60-70% to locations nationwide is required
  • A valid driver's license and the ability to drive to monitoring sites
  • Minimum 1 year healthcare-related work experience preferred
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • 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

  • Dallas Campus Overview
  • 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.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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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