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Cra International information

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$11K

$79.4K

$137.5K

How much do cra international jobs pay per year?

As of Sep 6, 2026, the average yearly pay for cra international 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 is CRA International?

CRA International, also known as Charles River Associates, is a global consulting firm that provides economic, financial, and management consulting services. They help businesses, law firms, and governments solve complex problems related to litigation, regulatory matters, business strategy, and more. Their consultants are experts in areas such as antitrust, finance, energy, life sciences, and intellectual property. CRA International is known for delivering rigorous analysis and objective advice to support decision-making in high-stakes situations.

What skills and qualifications are needed to thrive as an economic consultant at CRA International?

To thrive as an economic consultant at CRA International, you need strong analytical, quantitative, and research skills, typically supported by a degree in economics, finance, or a related field. Proficiency in data analysis tools such as Excel, Stata, or R, and familiarity with economic modeling software are commonly required. Outstanding communication, critical thinking, and teamwork abilities help consultants effectively present findings and collaborate with clients and colleagues. These skills are vital for delivering data-driven insights, supporting complex litigation cases, and providing high-value consulting services.

What types of projects do consultants typically work on at CRA International?

At CRA International, consultants are often engaged in a wide range of projects, including economic analysis for litigation, regulatory consulting, and strategic advisory work across industries such as finance, energy, and healthcare. This project variety allows consultants to develop expertise in different sectors, learn new analytical methodologies, and collaborate with diverse teams of experts. The exposure to multiple case types and client issues not only keeps the work intellectually stimulating but also accelerates professional growth and opens up opportunities for specialization or advancement within the firm.

What is the difference between Cra International vs Cra Analyst?

AspectCra InternationalCra Analyst
Required CredentialsBachelor's degree, relevant certifications (e.g., CRA certification)Bachelor's degree, often pursuing CRA certification
Work EnvironmentClinical research organizations, pharmaceutical companiesClinical trial sites, research organizations
Employer & Industry UsageUsed by CROs and pharma companies for overseeing trialsUsed at trial sites or research firms to monitor studies
Common Search & ComparisonOften compared for roles in clinical trial managementCompared as entry-level or site-based clinical research roles

The main difference between Cra International and Cra Analyst lies in their work environment and responsibilities. Cra International typically refers to professionals working for CROs or pharmaceutical companies managing multiple trials, while Cra Analysts are often based at clinical sites or research organizations focusing on data collection and trial monitoring. Both roles require similar credentials, but their scope and daily tasks differ significantly.

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The most popular types of Cra International jobs are:

What job categories do people searching Cra International jobs look for?

The top searched job categories for Cra International jobs are:

Cra International jobs near you
Infographic showing various Cra International job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Medpace, Inc.

Remote

Other

Medical, Retirement, PTO

Re-posted yesterday

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research

Job description

Job Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
This is an exciting home-based opportunity for clinical research professionals with at least two years of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE® Training Program, you will receive the training needed to become a fully resourced CRA. You will also have the opportunity to earn a generous travel bonus, in addition to a competitive salary.
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
  • Experience as a Clinical Research Coordinator (minimum 2 years)
  • Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
  • A valid driver's license and the ability to drive to monitoring sites
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

#LI-Remote
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

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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

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