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Clinical Development Scientist Jobs in Ohio (NOW HIRING)

Philips Iberica SAU

Clinical Affairs Director

Orange, OH · On-site

$171 - $273/hr

Drive the integration of scientific evidence to support product development, lifecycle management, and commercialization efforts. * Direct cross-functional collaboration among Clinical Affairs, R&D, ...

New

Medpace, Inc.

Clinical Nurse-2nd shift

Cincinnati, OH · On-site

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

Medpace, Inc.

Clinical Nurse-2nd shift

Cincinnati, OH · On-site

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

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Showing results 41-60

All JobsClinical Development Scientist JobsClinical Development Scientist Jobs in Ohio

Clinical Development Scientist information

See Ohio salary details

$26

$52

$77

How much do clinical development scientist jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical development scientist in Ohio is $52.05, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $64.90 per hour, depending on experience, location, and employer.

What does a clinical development scientist do?

A Clinical Development Scientist is responsible for designing, planning, and overseeing clinical trials that test new drugs, therapies, or medical devices. They collaborate with cross-functional teams to ensure that clinical studies are scientifically sound, compliant with regulations, and aligned with strategic objectives. Their work involves protocol development, data analysis, and interpretation of results to support regulatory submissions and product approvals. Ultimately, they play a key role in bringing safe and effective treatments to patients.

What skills and qualifications are needed to be a clinical development scientist?

To thrive as a Clinical Development Scientist, you need a solid background in life sciences, clinical research methodologies, and drug development, often supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory requirements, clinical trial management systems (CTMS), and data analysis tools is essential. Strong analytical thinking, attention to detail, and effective communication skills help you collaborate cross-functionally and drive successful clinical studies. These skills ensure rigorous study design, regulatory compliance, and effective advancement of new therapies through clinical pipelines.

How does a clinical development scientist collaborate with cross-functional teams during a clinical trial?

Clinical Development Scientists play a central role in coordinating with various teams such as clinical operations, regulatory affairs, data management, and biostatistics throughout a clinical trial. They ensure that clinical protocols are scientifically sound and align with regulatory requirements, while also facilitating clear communication between departments to address study challenges and maintain timelines. By serving as the scientific point of contact, they help integrate input from multiple stakeholders, support troubleshooting during trial execution, and contribute to the preparation of study documents and data analysis.

What is the difference between Clinical Development Scientist vs Clinical Research Associate?

AspectClinical Development ScientistClinical Research Associate
Required credentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's in Life Sciences or related field, often with certification in clinical trials
Work environmentDesigning and planning clinical trials, collaborating with teamsMonitoring clinical trials at sites, ensuring protocol compliance
Employer and industry usagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, research institutions
Common search and comparison intentUnderstanding roles in clinical developmentMonitoring and managing clinical trial sites

The Clinical Development Scientist focuses on designing, planning, and analyzing clinical trials, working closely with research teams. In contrast, the Clinical Research Associate primarily monitors trial sites to ensure compliance and data integrity. Both roles are essential in clinical research but differ in responsibilities and daily tasks.

What are popular job titles related to Clinical Development Scientist jobs in Ohio?

For Clinical Development Scientist jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Clinical Development Scientist jobs in Ohio look for?

The top searched job categories for Clinical Development Scientist jobs in Ohio are:

Clinical Development Scientist jobs near you
Infographic showing various Clinical Development Scientist job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $108,263 per year, or $52 per hour.

Early Career Clinical Research Opportunities

Medpace, Inc.

Cincinnati, OH • On-site

$23.25 - $31/hr

Other

Medical, Retirement, PTO

Posted 28 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 74 rated research

Job description

Job Summary
We are seeking upcoming and recent life science graduates to join our team as a Research Coordinator. This is an entry-level position intended to develop a purposeful understanding of clinical research through direct mentorship from physicians, scientists, and industry-leading experts. If you have a passion for advancing science and accelerating the development of medical therapeutics, apply now!
What To Expect:
  • Continuous growth and development through industry renowned training & mentorship programs in an office-based environment
  • Well-defined career paths with clear advancement and mobility opportunities
  • A collaborative and interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust
  • Broad exposure to various therapeutic areas and types of research
  • Accessible and approachable management and leadership

Responsibilities
  • Develop a rich understanding of Good Clinical Practice guidelines and drug development regulations relating to clinical trial conduct
  • Contribute to the progression of clinical trials from study start-up through close-out across a broad range of therapeutic areas
  • Collaborate across internal functions, sponsor companies, and vendors to support clinical trial execution and conduct

Qualifications
  • Bachelor's degree in Life Sciences or a related field
  • Strong attention to detail
  • Willingness to learn and accept feedback
  • Excellent communication and presentation 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.

What Medpace employees say

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Hours and flexibility

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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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