1

Biotech Cra Jobs in Ohio (NOW HIRING)

Showing results 21-21

Biotech Cra information

See Ohio salary details

$10.5K

$75.5K

$130.7K

How much do biotech cra jobs pay per year?

As of Sep 5, 2026, the average yearly pay for biotech cra in Ohio is $75,520.00, according to ZipRecruiter salary data. Most workers in this role earn between $31,400.00 and $129,800.00 per year, depending on experience, location, and employer.

What is a Biotech CRA?

A Biotech Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials to ensure they are conducted according to regulatory guidelines, protocols, and good clinical practice (GCP). CRAs work for biotechnology companies, contract research organizations (CROs), or pharmaceutical firms, and they oversee the progress of clinical studies, verify data accuracy, and ensure participant safety. Their role often involves traveling to clinical trial sites, reviewing documentation, and liaising between site staff and sponsors. Biotech CRAs are essential in bringing new therapies and medical products to market safely and efficiently.

How does a Biotech Clinical Research Associate (CRA) typically collaborate with site staff and sponsors during a clinical trial?

A Biotech CRA serves as the primary point of contact between the sponsor and the clinical site, ensuring protocols are followed and data integrity is maintained. They regularly communicate with site staff to monitor progress, address issues, and provide training or clarification on study procedures. CRAs also report site performance and findings back to the sponsor, facilitating smooth collaboration and quick resolution of challenges. Building strong professional relationships and clear communication channels are key to success in this collaborative environment.

What are the key skills and qualifications needed to thrive as a Biotech Clinical Research Associate (CRA), and why are they important?

To thrive as a Biotech Clinical Research Associate, you need a strong background in life sciences, clinical trial processes, and regulatory guidelines, typically supported by a bachelor’s degree in a relevant field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and often certifications like ACRP or SOCRA are important. Excellent attention to detail, problem-solving abilities, and strong communication skills help you manage study sites and ensure protocol compliance. These skills are essential for maintaining data integrity, regulatory adherence, and the successful execution of clinical trials.

What is the difference between Biotech Cra vs Clinical Research Associate?

AspectBiotech CraClinical Research Associate
CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree in health sciences or related field, certifications often preferred
Work EnvironmentBiotech companies, laboratories, research facilitiesClinical trial sites, hospitals, research organizations
Industry UsageBiotech and pharmaceutical industries focusing on drug developmentClinical trial management across various healthcare settings
Job FocusSupporting biotech research, data collection, and regulatory complianceMonitoring clinical trials, ensuring protocol adherence, site management

Both roles involve research and data management, but Biotech CRAs focus on supporting biotech research projects within laboratories, while Clinical Research Associates primarily oversee clinical trial sites to ensure compliance and data integrity. Understanding these differences helps job seekers target the right roles in the biotech and clinical research industries.

What cities in Ohio are hiring for Biotech Cra jobs?

Cities in Ohio with the most Biotech Cra job openings:

Infographic showing various Biotech Cra job openings in Ohio as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 4% Part Time, 2% Temporary, and 6% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $75,520 per year, or $36.3 per hour.

Entry-Level Patient Recruitment Coordinator

Medpace, Inc.

Cincinnati, OH • On-site, Remote

$16.75 - $22/hr

Full-time

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

16th of 75 rated research


Job description

Job Summary

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Patient Recruitment Coordinator to join our Patient Recruitment team. This position will work both independently and with a team to accomplish tasks and projects that are instrumental to recruiting and retaining patients for our clinical research trials. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Implement various recruitment strategies for clinical research studies;
  • Work effectively with the Clinical Research Associate (CRA) to discuss recruitment strategies and enrollment targets;
  • Work effectively with Recruitment to develop recruitment plans and ideas for new and on-going studies;
  • Utilize our systems to track progress of media generated referrals and overall study enrollment;
  • Update study specific social media sites; and
  • Perform ad-hoc projects/tasks as needed.
Qualifications
  • Bachelors in Life Science or General Business
  • At least 1 year of business experience;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office programs; and
  • Attention to detail and excellent oral and written communication skills.
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 and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

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.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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