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Director Clinical Development Jobs in Washington

Director of Clinical Development

Gaithersburg, MD · On-site

$86K - $117K/yr

Director level MD with 2-5 years of experience within a pharmaceutical company environment required ... clinical development plans for oncology or autoimmune therapeutic areas Ability to author key ...

Otsuka is seeking an Director, Global Clinical Development (GCD) based remotely or in our Princeton, NJ or Rockville, MD offices, who will be responsible for the design and oversight of clinical ...

Coordinates and monitors the development of long-range plans and annual department budgets. * Works closely with leaders to ensure strategic goals are being communicated and met appropriately at each ...

Coordinates and monitors the development of long-range plans and annual department budgets. * Works closely with leaders to ensure strategic goals are being communicated and met appropriately at each ...

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Showing results 1-20

Director Clinical Development information

See Washington salary details

$56.6K

$143.4K

$240.1K

How much do director clinical development jobs pay per year?

As of Jul 31, 2026, the average yearly pay for director clinical development in Washington is $143,431.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,900.00 and $171,600.00 per year, depending on experience, location, and employer.

What does a Director of Clinical Development do?

A Director of Clinical Development oversees the planning, execution, and management of clinical trials to ensure the safety and efficacy of new therapies. They collaborate with cross-functional teams, regulatory agencies, and key stakeholders to design and implement clinical strategies. Their role includes protocol development, trial monitoring, and ensuring compliance with regulatory standards. Additionally, they analyze trial data, manage budgets, and contribute to the overall drug development process.

What are the most common challenges faced by a Director of Clinical Development?

Directors of Clinical Development often navigate challenges such as aligning multiple cross-functional teams, managing complex project timelines, and ensuring compliance with evolving regulatory standards globally. They may also need to address issues related to trial participant recruitment, data integrity, and budget management. Adapting quickly to shifting priorities while maintaining high ethical and scientific standards is crucial. Successful Directors leverage collaboration, proactive problem-solving, and their in-depth industry knowledge to overcome these challenges and deliver impactful clinical results.

What are the key skills and qualifications needed to thrive in the Director Clinical Development position, and why are they important?

A Director Clinical Development typically requires an advanced degree in life sciences or medicine, extensive experience in clinical research, and a strong understanding of regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are highly valued. Exceptional leadership, strategic thinking, and effective cross-functional communication set outstanding candidates apart. These competencies ensure clinical programs are executed efficiently, ethically, and in alignment with organizational goals.

What are the most commonly searched types of Clinical Development jobs in Washington? The most popular types of Clinical Development jobs in Washington are:
What are popular job titles related to Director Clinical Development jobs in Washington? For Director Clinical Development jobs in Washington, the most frequently searched job titles are:
What cities in Washington are hiring for Director Clinical Development jobs? Cities in Washington with the most Director Clinical Development job openings:
Infographic showing various Director Clinical Development job openings in Washington as of July 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 85% In-person, 2% Hybrid, and 13% Remote job distribution, with an average salary of $143,431 per year, or $69 per hour.

Medical Director, Clinical Development, Endocrinology

Regeneron Pharmaceuticals

Washington, DC • Hybrid

$284K - $385K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

Medical Director, Clinical Development, Endocrinology

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

4 days a week on-site in Tarrytown, NY, Washington, D.C., or Cambridge, Massachusetts

Discover your role:

  • You guide the Global Clinical Study Team to deliver high-quality trials on time.
  • You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance
  • You lead clinical study and protocol development and present to internal and external stakeholders.
  • You provide clinical and scientific leadership for data review, study reports, and publications.
  • You work closely with cross-functional partners to advance program goals and key deliverables.
  • You collaborate with discovery teams to help shape future targets and development opportunities in the field.

This role requires:

  • An M.D. or equivalent with board eligibility or board certification in Endocrinologystrongly preferred; relevant experience can be acceptable.
  • At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)
  • Experience in rare disease drug development strongly preferred
  • Previous interactions with regulatoryagencies or common technical document (CTD or "dossier") submission in an ICH region is an advantage

#MDJobsCD, #MDJobs, #GDTherapeuticJobs, #Obesity

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$284,900.00 - $385,700.00

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