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Cro Legal Jobs (NOW HIRING)

Production Technician III-I/CRO

Sallis, MS · On-site

$16.75 - $21/hr

Onsite Legal Entity: Entergy Mississippi, LLC *This position may be filled as a Production ... Production Technician CRO : 5+ years of experience in a CCGT facility in an Operations or ...

Production Technician III-I/CRO

Sallis, MS

$16.75 - $21/hr

Onsite Legal Entity: Entergy Mississippi, LLC *This position may be filled as a Production ... Production Technician CRO : 5+ years of experience in a CCGT facility in an Operations or ...

Collaborate with various departments at PSI CRO, including Clinical Operations, Regulatory, and Legal, to ensure the successful implementation of the referral process across all projects.

Legal Counsel

New York, NY · On-site

$150K - $220K/yr

Legal Counsel As a key member of our growing legal team, you will be at the center of our US ... Sanj (CRO): PhD in AI (Gatsby Unit, UCL), ex-Huawei R&D, former lead at Magic Carpet AI (acquired)

Collaborate with various departments at PSI CRO, including Clinical Operations, Regulatory, and Legal, to ensure the successful implementation of the referral process across all projects.

Legal Counsel

New York, NY · On-site

$150K - $220K/yr

Legal Counsel As a key member of our growing legal team, you will be at the center of our US ... Sanj (CRO): PhD in AI (Gatsby Unit, UCL), ex-Huawei R&D, former lead at Magic Carpet AI (acquired)

Legal Counsel

Golden Valley, MN · On-site

$128.50K - $238.60K/yr

We have an opportunity for a Legal Counsel to join our Golden Valley, MN team. You will principally support our Flow Business Unit, as well as provide support to other legal and compliance ...

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Showing results 1-20

Cro Legal information

See salary details

$21K

$55.4K

$90K

How much do cro legal jobs pay per year?

As of May 30, 2026, the average yearly pay for cro legal in the United States is $55,419.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $62,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a CRO Legal professional, and why are they important?

To thrive as a CRO Legal professional, you need a solid background in law, regulatory compliance, and risk management, often supported by a law degree and relevant certifications. Familiarity with legal research databases, contract management systems, and compliance tracking tools is typically required. Strong analytical thinking, attention to detail, and effective communication skills are essential soft skills for this role. These competencies ensure that organizations remain compliant, mitigate legal risks, and effectively manage regulatory challenges.

What are some common challenges faced by legal professionals working in the CRO (Contract Research Organization) industry?

Legal professionals in CROs often navigate the complexities of international regulations, contract negotiations, and compliance with evolving clinical trial requirements. Balancing the interests of sponsors, research sites, and regulatory bodies can be challenging, particularly when timelines are tight and stakes are high. Additionally, the fast-paced nature of the CRO environment requires adaptability and strong communication skills to ensure legal and ethical standards are consistently met while supporting project teams.

What are CRO Legal professionals?

CRO Legal professionals are legal experts who work within or advise Contract Research Organizations (CROs), which are companies that provide research services to the pharmaceutical, biotechnology, and medical device industries. Their main role is to ensure that the organization's research operations comply with all relevant laws, regulations, and industry standards. They draft and review contracts, manage intellectual property issues, support regulatory submissions, and advise on data privacy, ethics, and compliance matters. CRO Legal professionals play a critical role in minimizing legal risks and facilitating smooth clinical trial operations.

What is the difference between Cro Legal vs Clinical Research Coordinator?

AspectCro LegalClinical Research Coordinator
Required CredentialsLegal education, law degree, or legal certificationsBachelor's degree in health sciences, life sciences, or related field; certification often preferred
Work EnvironmentLegal offices, law firms, corporate legal departmentsHospitals, research institutions, clinical trial sites
Employer & Industry UsageLegal industry, pharmaceutical companies, biotech firmsHealthcare, academic research, clinical trial organizations
Common Search & Comparison IntentUnderstanding legal roles in clinical researchManaging clinical trial processes and participant coordination

While Cro Legal focuses on legal aspects within the clinical research industry, Clinical Research Coordinators handle the day-to-day management of clinical trials. Both roles are essential but differ in credentials, work environment, and industry focus.

Infographic showing various Cro Legal job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 84% Full Time, 14% Part Time, and 1% Contract. Highlights an 20% Physical, and 80% Remote job distribution, with an average salary of $55,419 per year, or $26.6 per hour.
Legal Assistant - Site Contracts

Legal Assistant - Site Contracts

Medpace, Inc.

Cincinnati, OH

Other

Medical, PTO

Posted 23 days ago


Medpace rating

8.4

Company rating: 8.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

14th of 56 rated research


Job description

Job Summary

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Legal Assistant to join our Clinical Operations team. This position will work in a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you can develop and grow your career even further, then this is the opportunity for you. *This position is fully office-based in Cincinnati, OH. 

Responsibilities
  • Provide day-to-day departmental/project support with general contract administrative duties;
  • Assist with preparation of final contract documentation, liaising with study teams and study centers;
  • Perform other administrative tasks as needed to support successful contract negotiation/execution;
  • Conduct quality control reviews of departmental documents as necessary;
  • Maintain databases/project specific status reports.
Qualifications
  • Minimum High school degree, Associates degree preferred;
  • Experience with contracts or legal work preferred;
  • Good organizational and prioritization skills and attention for details;
  • Excellent oral and written communication skills;
  • Willing to work fully office-based; and
  • Computer literacy (Microsoft Office Package). 
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.

Cincinnati Perks

  • Cincinnati 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 local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

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

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