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Associate Medical Director Clinical Development Jobs in Ohio

Medical Director (Oncology)

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Medical Director (Oncology)

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Nephrologist - Medical Director

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Medical Director, Psychiatry

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Medical Director, Psychiatry

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Medical Director, Neurologist

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

Medical Director, Neurologist

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

The Medical Director will also be involved in the development of new clinical projects, including ... Manage safety issues in clinical trials and work closely with associates in evaluation and ...

$102.94 - $148.69/hr

Director Clinical Development and Medical Assessment (w/m/d) Bad Vilbel, Deutschland STADA Arzneimittel AG - Global Specialty Development Dieser Auftrag motiviert uns bei STADA jeden Tag aufs Neue, ...

$217.98 - $272.48/hr

## Country Medical Director, GermanyApplylocations: Germany Remotetime type: Full timeposted on ... Clinical Development, and Corporate Affairs. This includes aligning priorities, facilitating ...

Showing results 21-40

Associate Medical Director Clinical Development information

See Ohio salary details

$71.8K

$156.7K

$249.6K

How much do associate medical director clinical development jobs pay per year?

As of Aug 19, 2026, the average yearly pay for associate medical director clinical development in Ohio is $156,672.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,500.00 and $190,100.00 per year, depending on experience, location, and employer.

What does an associate medical director clinical development do?

An Associate Medical Director in Clinical Development oversees and supports the planning, execution, and monitoring of clinical trials for new drugs or medical therapies. They collaborate with cross-functional teams to ensure that studies are scientifically sound, ethically conducted, and in compliance with regulatory standards. Their responsibilities often include protocol development, data review, safety monitoring, and contributing to regulatory submissions. Additionally, they may interact with key opinion leaders and provide medical expertise throughout the clinical development process.

What are the key skills and qualifications needed to thrive as an associate medical director clinical development?

To thrive as an Associate Medical Director Clinical Development, you need a medical degree (MD, DO, or equivalent), clinical experience, and a strong understanding of clinical trial design and regulatory requirements. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and relevant certifications such as GCP (Good Clinical Practice) are highly valuable. Exceptional leadership, strategic thinking, and communication skills help you effectively collaborate with cross-functional teams and manage complex projects. These competencies ensure the safe, efficient, and compliant execution of clinical trials that drive successful drug development.

What are the primary challenges faced by an associate medical director clinical development when managing cross-functional project teams?

One of the main challenges for an Associate Medical Director in Clinical Development is effectively coordinating and communicating with diverse cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics. Balancing scientific objectives with operational feasibility often requires strong leadership and negotiation skills. Additionally, managing multiple priorities while ensuring adherence to timelines and regulatory standards can be demanding. Success in this role depends on fostering collaboration, maintaining clear communication, and proactively addressing project risks.

What is the difference between Associate Medical Director Clinical Development vs Medical Director Clinical Development?

AspectAssociate Medical Director Clinical DevelopmentMedical Director Clinical Development
Required CredentialsMD or DO, relevant clinical experience, often with some industry exposureMD or DO, extensive clinical and industry experience, leadership credentials
Work EnvironmentSupportive, collaborative teams within pharmaceutical or biotech companiesLeadership roles overseeing clinical development strategies
Employer & Industry UsageCommon in pharmaceutical and biotech firms, early to mid-stage clinical teamsSenior clinical leadership in similar settings, overseeing multiple projects
Search & Comparison IntentUnderstanding entry to mid-level clinical development rolesClarifying senior clinical leadership positions

The Associate Medical Director Clinical Development typically supports clinical trial activities and assists in development strategies, often with less seniority. The Medical Director Clinical Development holds a higher leadership role, overseeing entire clinical programs and making strategic decisions. Both roles require medical credentials and industry experience, but the Medical Director has broader responsibilities and authority.

What are popular job titles related to Associate Medical Director Clinical Development jobs in Ohio?

For Associate Medical Director Clinical Development jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Associate Medical Director Clinical Development jobs in Ohio look for?

The top searched job categories for Associate Medical Director Clinical Development jobs in Ohio are:

What cities in Ohio are hiring for Associate Medical Director Clinical Development jobs?

Cities in Ohio with the most Associate Medical Director Clinical Development job openings:

Nephrologist - Medical Director

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 6 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research


Job description

Job Summary

We are seeking a Nephrologist- Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in all Therapeutic Areas.

**All Medical Directors have hybrid WFH flexibility. This role also has the ability to be fully remote with the right experience**.

Responsibilities
  • Provide medical management and expertise for clinical trials;
  • Contribute medical expertise to study reports, regulatory documents, and manuscripts;
  • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;
  • Participate in new business development through involvement in proposal and sponsor meetings as requested;
  • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;
  • Follow specific research related protocol and lead others in strict adherence to the policies.
Qualifications
  • Must have an M.D., specialization in Nephrology
  • Must be eligible to obtain a medical license
  • Board certification preferred
  • Prior clinical trial research experience preferred
  • Previous experience in pharmaceutical-related clinical research is preferred.

 Travel: up to 20%

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


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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