Job DescriptionRole and Responsibilities:We are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics -Oncology (QP2 Oncology) team as
Senior Director, Quantitative Systems Pharmacology (QSP). QP2 Oncology is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-preclinical candidate (PCC) selection through registration.
Our Senior Directors are recognized experts in quantitative drug development and possess a deep, integrated understanding of both the science and the strategic, end-to-end dimensions of oncology drug development. Reporting directly to Executive Director and Section Head, QP2 Oncology, the Senior Director will provide leadership and scientific oversight to all QSP and mechanistic modeling efforts across the oncology portfolio.
Primary Responsibilities- Lead and shape the QSP strategy across the oncology portfolio, ensuring alignment with program goals and organizational priorities.
- Lead, mentor, and develop a team of quantitative scientists in a matrixed role.
- Work in close collaboration with QP2 Oncology team, preclinical DMPK and modeling teams, biologists, clinicians, and other line functions to utilize mechanistic/ QSP modeling for dose selection, combination strategies and clinical trial design.
- Ensure high-quality, regulatory grade QSP deliverables for internal decisions, submissions, and scientific advice meetings.
- Contribute to regulatory strategy through preparation of QSP reports, briefing documents, and presentations.
- Foster a culture of scientific rigor, excellence, collaboration, and innovation and develop best practices for QSP modeling.
- Partner with senior leaders in Translational Modeling, Discovery and Clinical Development to define modeling strategies that influence program design and key decisions.
- Represent the company at scientific conferences, external collaborations, consortia, and industry working groups.
- Stay at the forefront of emerging methodologies in QSP and promote innovation.
- Manage activities related to budget planning, QSP vendor identification and outsourcing of QSP analyses and contract requisitions.
Minimum education required:- Ph.D., with at least ten years of pharmaceutical drug development experience relating to: systems pharmacology, systems biology, PKPD, mathematics, chemical/biomedical engineering or related field.
- Masters or PharmD, with at least fifteen years of experience, where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
Required Experience:- Extensive and in-depth experience in developing mechanistic PK-PD models and QSP models for decision making in early and late-stage clinical development.
- Demonstrated ability to lead an interdisciplinary team or taskforce, and/or to oversee the work of others.
- Oncology therapeutic area or disease knowledge
- Experience with mechanistic modeling for antibody drug conjugates (ADCs) and/ or T-cell engagers in conjunction with immune-axis will be preferred.
- Experience with modeling and simulation packages or programming languages (e.g., MATLAB, R, SimBiology, Python)
- Experience working with external QSP vendors.
- Experience in utilizing QSP modeling in IND, NDA and other submissions to global regulatory agencies.
- An exemplary record of increasing responsibility, independence, and demonstrated impact in driving drug development decisions through application of mechanistic model-based approaches.
- Proficiency in written and verbal communication, interdisciplinary collaboration, and problem scoping and planning.
Required Skills:Business Intelligence (BI), Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Machine Learning (ML), Software Development, Stakeholder Relationship Management, Waterfall Model
Preferred Skills:Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job DescriptionThe remote position is only applicable for those that are not within commutable distance to primary sites noted in posting. If commutable, the position will be hybrid. Please note that standard commute is (less than)
US and Puerto Rico Residents Only:The salary range for this role is
$210,400.00 - $331,100.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
Employee Status: Regular
Relocation:Domestic
VISA Sponsorship:Yes
Travel Requirements:10%
Flexible Work Arrangements:Remote
Shift:1st - Day
Valid Driving License:No
Hazardous Material(s):N/A
Job Posting End Date:09/11/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
