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Director Metabolism Jobs (NOW HIRING)

Executive Director, DMPK Location: Exton, PA Reports to : VP, DMPK Frontage Laboratories Inc. is an ... Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety ...

Senior Director, ADME

Conshohocken, PA · On-site

$256 - $313/hr

## Senior Director, ADMEApplylocations: PA - Conshohocken - Officetime type: Full timeposted on ... This individual will bring deep expertise in drug metabolism, with working knowledge across broader ...

Senior Director, ADME

Conshohocken, PA · On-site

$256 - $313/hr

Senior Director, ADME This role is primarily responsible for nonclinical ADME strategy and ... This individual will bring deep expertise in drug metabolism, with working knowledge across broader ...

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Director Metabolism information

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$57K

$186.4K

$331K

How much do director metabolism jobs pay per year?

As of Aug 11, 2026, the average yearly pay for director metabolism in the United States is $186,382.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,500.00 and $249,500.00 per year, depending on experience, location, and employer.

What is the difference between Director Metabolism vs Metabolism Scientist?

AspectDirector MetabolismMetabolism Scientist
CredentialsAdvanced degrees (PhD, MD), leadership experienceTypically PhD or Master's in biochemistry, molecular biology
Work EnvironmentStrategic planning, team management, cross-department collaborationLaboratory research, data analysis, experimental design
Industry UsagePharmaceutical, biotech companies, research institutionsResearch labs, academic institutions, biotech firms

While both roles focus on metabolism, the Director Metabolism oversees strategic projects and manages teams, whereas the Metabolism Scientist conducts laboratory research and experiments. The director role involves leadership and planning, while the scientist role emphasizes technical expertise and experimental work.

What are the typical collaboration points between a director of metabolism and other departments in a pharmaceutical company?

As a Director of Metabolism, you will frequently collaborate with teams such as medicinal chemistry, pharmacokinetics, toxicology, and clinical operations. These interactions are crucial for designing experiments, interpreting metabolic data, and ensuring seamless progression of drug candidates through the development pipeline. Regular cross-functional meetings and project update discussions are common, requiring strong communication and leadership skills to align goals and timelines across departments. This collaborative environment not only enhances scientific outcomes but also offers valuable exposure to diverse areas within drug development.

What are the key skills and qualifications needed to thrive as a director of metabolism, and why are they important?

To thrive as a Director of Metabolism, you need an advanced degree (PhD, MD, or PharmD) in a life science field, deep expertise in metabolic diseases, and a proven track record in biomedical research or drug development. Familiarity with laboratory techniques, data analysis platforms, and regulatory requirements, as well as experience with project management tools, is typically required. Strong leadership, cross-functional collaboration, and strategic thinking are crucial soft skills for guiding teams and advancing research goals. These skills ensure effective oversight of complex projects, scientific innovation, and successful translation of research into therapeutic solutions.

What does a director of metabolism do?

A Director of Metabolism typically leads research and development efforts focused on metabolic diseases, such as diabetes or obesity, within pharmaceutical or biotechnology companies. They oversee scientific teams, design and implement research strategies, and collaborate with other departments to advance drug discovery or clinical programs. This role also involves staying current with scientific advances, managing budgets, and ensuring compliance with regulatory standards. Directors of Metabolism play a crucial role in bringing new therapies from concept to clinical use.
More about Director Metabolism jobs
What cities are hiring for Director Metabolism jobs? Cities with the most Director Metabolism job openings:
What are the most commonly searched types of Metabolism jobs? The most popular types of Metabolism jobs are:
What states have the most Director Metabolism jobs? States with the most job openings for Director Metabolism jobs include:
Infographic showing various Director Metabolism job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $186,382 per year, or $89.6 per hour.

Senior Medical Director, Clinical Development, Cardiovascular/Metabolism

Regeneron Pharmaceuticals

Cambridge, MA • On-site

$333K - $450K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 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

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 Senior Medical Director, Clinical Development to join our Cardiovascular/Renal/Metabolism team, supporting programs focused on obesity and related comorbidities. In this role, you will serve as Scientific and Medical Lead for clinical team(s), guiding development strategy and regulatory submissions while collaborating with Operational Leads, discovery teams, and Global Patient Safety. This role reports to an Executive Medical Director, Internal Medicine. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Tarrytown, NY, Cambridge, MA, or Warren, NJ

  • Travel: 10% to relevant conferences

Discover your role:

  • Develop innovative clinical strategies to shorten development cycles amid an evolving regulatory landscape

  • Design efficient, robust Phase 2/3 programs

  • Partner with discovery teams to inform next-generation targets and lead Phase 1 clinical testing plans for initial PK/PD and safety characterization

  • Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance

  • Act as medical expert and leader in interactions with external stakeholders

  • Plan and execute publication and clinical communication strategy, and contribute to key external presentations

  • Ensure the quality of clinical documents, including investigator brochures, protocols, study reports, and regulatory submission materials

This role requires:

  • MD or equivalent advanced medical degree

  • Clinical training in Endocrinology or Cardiology (board certified or eligible) strongly preferred

  • Minimum of 4 years of relevant clinical development experience in industry, including protocol design, study start-up, and study team execution

  • Experience with regulatory filings and health authority interactions preferred

#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs, #CVMet, #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)

$333,300.00 - $450,900.00

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