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$13K

$232.4K

$357K

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

As of Sep 4, 2026, the average yearly pay for medical director clinical development in the United States is $232,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $198,000.00 and $284,500.00 per year, depending on experience, location, and employer.

What does a medical director clinical development do?

A Medical Director of Clinical Development is responsible for overseeing the planning, execution, and management of clinical trials for new drugs or medical products. They work closely with cross-functional teams, such as regulatory affairs, clinical operations, and research scientists, to ensure that clinical studies are designed effectively and conducted in compliance with regulatory standards. Their role also includes reviewing and interpreting clinical data, providing medical expertise, and contributing to the overall strategy for product development. Medical Directors play a crucial role in ensuring the safety and efficacy of new therapies before they reach the market.

How does a medical director clinical development typically collaborate with cross-functional teams during a clinical trial?

As a Medical Director in Clinical Development, you will regularly collaborate with cross-functional teams such as clinical operations, regulatory affairs, biostatistics, data management, and pharmacovigilance. Your role involves providing medical and scientific guidance, ensuring protocol adherence, and addressing safety or efficacy concerns throughout the trial. Effective communication and teamwork are essential for aligning on trial objectives, managing timelines, and resolving any emerging issues. This collaborative environment fosters a comprehensive approach to advancing clinical programs and supports the successful execution of clinical trials.

What are the key skills and qualifications needed to thrive as a medical director clinical development, and why are they important?

To thrive as a Medical Director Clinical Development, you need an advanced medical degree (MD or equivalent), extensive clinical research experience, and a deep understanding of regulatory requirements and drug development processes. Familiarity with electronic data capture systems, clinical trial management software, and GCP/ICH guidelines is typically required. Strong leadership, strategic thinking, and exceptional communication skills help drive multidisciplinary teams and manage complex projects. These skills ensure the safe, efficient, and compliant progression of clinical programs from conception through regulatory approval.

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

AspectMedical Director Clinical DevelopmentMedical Scientist
Required CredentialsMD or DO, clinical research experience, industry certificationsMD, PhD, or equivalent, research-focused
Work EnvironmentPharmaceutical companies, biotech firms, clinical trial oversightResearch institutions, academia, laboratories
Employer & Industry UsageCommonly employed in industry to oversee clinical developmentPrimarily in research and academia, less in industry

The Medical Director Clinical Development typically oversees clinical trials and ensures regulatory compliance within the industry, requiring medical credentials and industry experience. Medical Scientists focus on research and discovery, often working in labs or academic settings. While both roles require advanced degrees, their work environments and primary responsibilities differ significantly.

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Medical Director Clinical Development jobs near you
Infographic showing various Medical Director Clinical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $232,369 per year, or $111.7 per hour.

Medical Director, Clinical Development

Kailera Therapeutics, Inc.

Waltham, MA • On-site

Full-time

Re-posted 20 days ago

Job description

What You'll Do:

We are seeking an experienced, highly motivated Medical Director, Clinical Development to join our growing team. This individual will play a pivotal role in designing and executing clinical development programs that advance our pipeline of innovative therapeutics. The successful candidate will bring strong clinical insight, a deep understanding of drug development in a biotech setting, and a proven ability to work cross-functionally in a dynamic, fast-paced environment.

Responsibilities:

  • Responsible for medical monitoring/reporting and safety activities
  • Provide medical leadership in the design, planning, and execution of clinical development strategies across multiple studies
  • Acts as the medical contact at the company for clinical/medical issues
  • Interprets, reports, and prepares oral and written results of product research, in concert with senior clinical personnel
  • Serve as the medical expert for assigned assets studies
  • Contribute to regulatory interactions and strategy, including IND/CTA submissions and briefing packages
  • Collaborate and work closely with Clinical Operations to ensure appropriate site selection, patient recruitment strategies, and high-quality trial execution
  • Oversee and support data interpretation, analysis, and clinical study reports
  • Work closely with internal stakeholders, including Regulatory, Safety, CMC, Medical Affairs, and Translational Science teams
  • Partner with external collaborators, KOLs, CROs, and investigators
  • Support scientific publications, conference presentations, and other external communications
  • Participate in safety review meetings and provide clinical input into adverse event evaluation and reporting

Required Qualifications:

  • 3+ years of industry experience in clinical development, preferably in a biotech or small pharma environment
  • Hands-on experience designing and executing clinical trials
  • Understanding of GCP, clinical trial design, regulatory requirements, and safety monitoring
  • Excellent written and verbal communication skills, including protocol and regulatory document writing
  • Demonstrated ability to engage with KOLs, investigators, and cross-functional teams
  • Can work independently, self-starter attitude
  • Advanced PowerPoint skills; working knowledge of Excel and other commonly used clinical systems/tools
  • Ability to manage multiple studies and deadlines in a fast-paced environment
  • Must be exceptionally detail oriented

Preferred Qualifications:

  • Experience in cardiometabolic therapeutic area is advantageous
  • Proven track record of contributing to IND submissions and global regulatory filings is a strong plus

Education:

  • MD or equivalent is required

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