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Clinical Development Biotech Jobs in Ohio (NOW HIRING)

Medpace

Software Development Co-Op - Fall 2026

Cincinnati, OH · On-site

$35.25 - $48.25/hr

Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology Founded in 1992, the company is headquartered in Cincinnati, USA, with a ...

Medpace

SAS Programmer - Experienced

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization (CRO) that provides clinical development services to the biotechnology, pharmaceutical, and medical device industries. They are ...

Medpace

Junior Network Engineer

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization (CRO) that provides clinical development services to the biotechnology, pharmaceutical, and medical device industries. They are ...

Medpace

Junior Data Engineer

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization (CRO) providing clinical development services to the biotechnology, pharmaceutical, and medical device industries. They are seeking a ...

Medpace

Senior Data Engineer

Cincinnati, OH · On-site

$103K - $140K/yr

Medpace is a full-service clinical contract research organization (CRO) providing clinical development services to the biotechnology, pharmaceutical, and medical device industries. The Senior Data ...

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Clinical Development Biotech information

What is clinical development in biotech?

Clinical development in biotech refers to the process of testing new drugs or therapies in human participants to determine their safety and effectiveness. This phase follows preclinical research and involves multiple stages of clinical trials, from Phase I (safety) to Phase III (efficacy and monitoring of side effects). Clinical development professionals coordinate the design, implementation, and analysis of these studies, ensuring compliance with regulatory standards. Their work is crucial in bringing innovative treatments from the laboratory to patients. Success in this field requires knowledge of medical science, regulatory guidelines, and project management.

What are the typical challenges faced by professionals working in clinical development within the biotech industry?

Professionals in clinical development for biotech companies often encounter challenges related to navigating complex regulatory requirements, managing tight timelines, and ensuring robust data quality across clinical trials. Additionally, frequent cross-functional collaboration is needed, as teams work closely with regulatory affairs, medical affairs, and data management to drive studies forward. Adapting to evolving scientific advancements and shifting project priorities are also common, so flexibility and strong communication skills are essential for success in this fast-paced environment.

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

AspectClinical Development BiotechClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, relevant certificationsBachelor's in life sciences, often with CRA certification
Work EnvironmentPharmaceutical/biotech companies, labs, clinical trial teamsMonitoring sites, clinical trial sites, sponsor offices
Employer & Industry UsageBiotech firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, research organizations
Common Search & ComparisonYesYes

The Clinical Development Biotech role focuses on planning and managing clinical trials within biotech companies, often involving protocol development and regulatory submissions. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity. While both roles require similar educational backgrounds and certifications, their daily responsibilities and work environments differ, with the former being more involved in trial design and the latter in trial oversight.

What are the key skills and qualifications needed to thrive as a Clinical Development professional in biotech, and why are they important?

To thrive in Clinical Development within biotech, you need a strong background in life sciences, clinical trials management, and regulatory compliance, often supported by an advanced degree (e.g., PhD, PharmD, or MD). Proficiency with clinical trial management systems (CTMS), data analysis tools, and familiarity with ICH-GCP guidelines and FDA regulations are typically required. Strong project management, communication, and problem-solving skills help navigate complex studies and multidisciplinary teams. These competencies are essential to ensure safe, efficient, and compliant development of new therapies from concept to market.
What are popular job titles related to Clinical Development Biotech jobs in Ohio? For Clinical Development Biotech jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Clinical Development Biotech jobs in Ohio look for? The top searched job categories for Clinical Development Biotech jobs in Ohio are:
What cities in Ohio are hiring for Clinical Development Biotech jobs? Cities in Ohio with the most Clinical Development Biotech job openings:
Clinical Development Biotech jobs near you
Clinical Application Administrator - Imaging

Clinical Application Administrator - Imaging

Medpace

Cincinnati, OH • On-site

Full-time

Re-posted 20 days ago

Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

14th of 59 rated research

Job description

Job Summary:
Medpace is a full-service clinical contract research organization (CRO) that provides clinical development services to the biotechnology, pharmaceutical, and medical device industries. The Clinical Application Administrator – Imaging role involves troubleshooting and providing support for internal software applications, collaborating with teams to resolve user issues, and delivering training for medical imaging applications.
Responsibilities:
• Act as a liaison between end users and application development teams while maintaining the interests of end users;
• Perform Medical Imaging commercial off-the-shelf applications maintenance, testing and validation
• Develop and implement approaches for the use of software applications as they apply to individual users and study teams;
• Create and maintain test cases, test plans, and other documentation for projects
• Ensure medical imaging system design, interface functionality, and clinical processes are coordinated and functioning effectively
• Deliver hands-on training for medical imaging applications to internal and external users
• Experience in the regulated healthcare industry is a plus
• Write SQL queries to interact with reporting database when setting up data feeds and integrations, and
• Perform other system-related tasks to meet company objectives.
Qualifications:
Required:
• Bachelor's degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field
• Good organizational skills, very detail oriented, flexible, and possess good communication skills
• Ability to interact with staff and external users from multiple countries
• Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project
• Competent in installation and troubleshooting of software
• Demonstrated ability to learn new technologies/applications
• Familiar with field’s concepts, practices, and procedures
Preferred:
• Experience in the regulated healthcare industry is a plus
Company:
Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology Founded in 1992, the company is headquartered in Cincinnati, USA, with a team of 5001-10000 employees. The company is currently Late Stage.

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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