Merck & Co, Inc

Principal Scientist, Pharmacokinetics

Merck & Co, Inc$176K — $277K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in a relevant scientific discipline with 8+ years of industry experience or MS with 12+ years.
  • Proven experience leading DMPK efforts in biologics and conjugate discovery teams.
  • Strong problem-solving and leadership skills with a self-driven mindset.
  • Proficiency in analyzing PK/PD data and translating it for drug discovery.
  • Demonstrated experience mentoring junior scientists, fostering diversity and inclusion.

Responsibilities

  • Serve as a project-team representative and expert in biologics drug discovery.
  • Design mechanistic studies to evaluate pharmacokinetic and metabolic properties.
  • Deliver timely, high-quality data deliverables to support project teams.
  • Author regulatory documents from first-in-human through filing.
  • Provide strategic DMPK guidance across multidisciplinary interfaces.
  • Contribute to departmental scientific strategies and initiatives.
  • Foster a culture of innovation, collaboration, and inclusion.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan options.
  • Paid holidays, vacation, and sick days.
  • Compassionate leave and other personal time off benefits.
Full Job Description

Job Description

Position description:

The SSF Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking an experienced Principal Scientist to contribute to our Company’s biologics, drug conjugates, and novel modality discovery and development pipeline. The ideal candidate will represent PDMB in project teams across multiple therapeutic areas, including Oncology, Cardiovascular metabolic disease, and Immunology. The candidate will develop a project team specific adaptable PDMB screening funnel and work closely with ADME, discovery bioanalytics and modeling partners to support lead identification/optimization, enable FIH translation, and compile non-clinical packages to support regulatory filing. The candidate will collaborate effectively with cross-functional partners in project teams to facilitate program progression through science-based decision making. The successful candidate must demonstrate the ability to work collaboratively in a fast-paced, dynamic environment and possess excellent scientific, interpersonal, and communication skills. Additionally, the candidate will influence DMPK strategy and new capability buildout.

Key Responsibilities of the Principal Scientist:

  • Project-team representative and subject matter expert for biologics drug discovery and development, including but not limited to drug conjugates, multi-specific biologics, and novel modalities. Contribute to overall team strategy and lead the formation and execution of team-specific PDMB workflow.

  • Design in vitro and in vivo mechanistic and translational studies to evaluate the pharmacokinetic and metabolic properties of therapeutic proteins, such as drug conjugates and other modalities, to influence drug design, lead selection, and drive PK/PD translations.

  • Accountable for providing timely and high-quality PDMB data deliverables to teams.

  • Author regulatory documents from FIH through registrational filing.

  • Partner across multidisciplinary interfaces and provide strategic DMPK guidance and support to drive new drug discovery and development.

  • Contribute to departmental scientific initiatives and strategies

  • Foster a high-performance culture of innovation, collaboration, engagement, self-accountability, and inclusion.

  • Stay abreast of external scientific advancements and contribute to the evaluation and implementation of new technologies and methodologies in DMPK for drug discovery.

Position qualifications:

Education Minimum Requirement:

  • Ph.D. in a relevant scientific discipline (e.g., Pharmacokinetics, Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Biology, or related field) with a minimum of 8 years of industry experience.

  • MS Degree with a minimum of 12 years of relevant experience.

Required Experience and Skills

  • Demonstrated team-facing experience leading DMPK efforts in biologics and conjugate discovery teams.

  • A proven track record of setting strategies and priorities and managing resources as an independent project-team representative within a highly dynamic and collaborative environment.

  • Proficiency in analyzing, interpreting, and providing context around data describing the DMPK and PKPD properties of therapeutic proteins; ability to extract preclinical PKPD/efficacy relationships and translate PKPD in humans.

  • Demonstrated ability to effectively collaborate with cross-functional teams and communicate DMPK findings to inform decision-making in drug discovery and development.

  • Strong problem-solving and leadership skills, highly motivated and self-driven with a keen interest in staying at the forefront of DMPK science and technology.

  • Demonstrated experiences in mentoring and training junior scientists with a mindset of fostering variety and inclusion within the scientific community.

Preferred Experience and Skills:

  • Prior experience with multiple therapeutic modalities (e.g. small molecules, peptides, etc) and/or novel modalities.

  • Prior experience evaluating the biodistribution of large molecules in preclinical species.

  • In-depth understanding and experience in discovery bioanalytical science, including immunoassay, LC/MS.  

  • Demonstrated experience in translatable in vitro cellular models, biophysics/biochemistry assays and/or in vivo models.

  • Understanding of modeling principles.

Required Skills:

ADME, Biochemical Analysis, Biophysics, Cross-Functional Teamwork, Detail-Oriented, Diversity and Inclusion (D&I), Drug Metabolism, Immunoassays, Innovation, Liquid Chromatography-Mass Spectrometry (LC-MS), Mentoring Staff, Pharmaceutical Sciences, Pharmacodynamics, Pharmacokinetics, PKPD Modeling, Therapeutic Proteins

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

The salary range for this role is

$176,200.00 - $277,300.00

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.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

07/22/2026

*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.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

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