Senior Director, ADME

Madrigalpharma; Conshohocken (Montgomery County); On-site; USD 256,000 - 313,000; Full time

Benefits offered by this job

Equity

Comprehensive benefits

401(k) with employer match

Job summary

Madrigal is seeking a Senior Director, ADME to provide scientific leadership for ADME activities across nonclinical and clinical programs. You will design strategies, oversee studies, and manage CROs to ensure data quality and regulatory readiness.

The role requires a PhD with 15+ years in ADME, deep metabolism expertise, and experience with PBPK modeling and human mass balance studies. Competitive compensation and comprehensive benefits apply to full-time staff.

Qualifications

• Ph.D. in Pharmacokinetics, Drug Metabolism, Pharmaceutical Sciences, or related field.
• 15+ years of ADME experience in pharmaceutical/biotech drug development.
• Experience supporting both nonclinical and clinical programs.

Responsibilities

• Serve as the ADME subject matter expert with deep metabolism expertise.
• Define and execute ADME strategies with cross-functional leads.
• Design, oversee, and interpret nonclinical ADME studies (in vitro/in vivo).
• Manage CROs including vendor selection, study design, and reports review.
• Author and review ADME sections of regulatory submissions (IND/CTA, NDA).

Skills

ADME expertise

Nonclinical ADME

PBPK modelling

CRO management

Education

PhD in Pharmacokinetics/Drug Metabolism/Pharmaceutical Sciences

Job description

## Senior Director, ADMEApplylocations: PA - Conshohocken - Officetime type: Full timeposted on: Posted 3 Days Agojob requisition id: JR\_000806Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration. To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.The Senior Director, ADME will provide technical leadership and execution for ADME activities supporting nonclinical and clinical development programs. This role is primarily responsible for nonclinical ADME strategy and oversight, while supporting Clinical Pharmacology and early clinical development as a subject matter expert.This individual will bring deep expertise in drug metabolism, with working knowledge across broader ADME disciplines, and will oversee all ADME studies conducted through CRO partners. The role requires strong hands-on scientific judgment to design, interpret, and integrate ADME data to support program decisions and regulatory submissions.**Key Responsibilities*** Serve as the ADME subject matter expert, with deep expertise in metabolism* Define and execute ADME strategies in collaboration with functional area leads* Design, oversee, and interpret nonclinical ADME studies (in vitro and in vivo)* Manage CROs, including vendor selection, study design, protocol development, and report review* Ensure ADME data are scientifically sound and aligned with regulatory expectations* Support clinical development through ADME input, including DDI risk assessment, PBPK modeling, and human ADME (mass balance) study design and interpretation* Integrate nonclinical and emerging clinical PK data to inform ADME strategy and study design* Author and review ADME sections of regulatory submissions (IND/CTA, NDA) and support regulatory interactions**Qualifications***Education & Experience** Ph.D. in Pharmacokinetics, Drug Metabolism, Pharmaceutical Sciences, or related discipline (or equivalent experience)* 15+ years of ADME experience in pharmaceutical or biotechnology drug development* Experience supporting both nonclinical and clinical programs*Technical Expertise** Deep expertise in drug metabolism (required)* Working knowledge of transporters and broader ADME sciences* Strong experience designing and interpreting ADME studies* Experience with PBPK modeling and human ADME (mass balance) studies preferred*Core Competencies** Strong scientific judgment and attention to detail* Hands-on, execution-focused approach* Effective communicator within technical and cross-functional teams* Ability to operate in a fast-paced, dynamic environmentMadrigal’s Total Rewards strategy is based on a biotech industry peer group comparator and is inclusive of base pay, bonus and equity. Our equity offers meaningful opportunity allowing our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.All employees receive equity, which we believe reinforces our ownership culture. Base salary is determined by several factors including the candidate’s qualifications, skills, education, experience, business needs and market demands. As of the date of this posting, a good faith estimate of the current pay scale for this position, applicable to all candidates, is $256,000 - $313,000 per year. We comply with all applicable minimum wage laws.All full-time employees receive equity, which reinforces our ownership culture and offers meaningful opportunity for our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization. Full-time employees are also eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans. We also offer additional voluntary benefits like supplemental life insurance, legal services, and other offerings. In addition, we offer mental health benefits through our Employee Assistance Program for employees and their family. The company also provides other benefits in accordance with applicable federal, state, and local laws. We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process. If you need assistance, please contact [e-mail]. Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law. Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established. Applications are being accepted on an ongoing basis and can be submitted through our Madrigal Careers site. *Please be aware that we have received reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals’ Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal’s name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.* *Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for or on behalf of Madrigal, we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks. Any questions regarding the legitimacy of job-related contacts can be directed to* *[e-mail]**.*