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Associate Principal Scientist, In Vivo Pharmacology, Oncology

Job in Boston, Suffolk County, Massachusetts, 02108, USA
Listing for: Merck
Full Time position
Listed on 2026-08-27
Job specializations:
  • Research/Development
    Research Scientist, Medical Science, Clinical Research, Oncology Care
Job Description & How to Apply Below

Associate Principal Scientist

Our Discovery Quantitative Biosciences (QB) In Vivo Pharmacology – Oncology team in Boston is searching for a collaborative and innovative Associate Principal Scientist with a strong background in Oncology In Vivo Pharmacology. The successful candidate will be an experienced In Vivo cancer biologist who will direct Oncology reverse-translational activities while serving as a key intellectual contributor in the conception and execution of Oncology drug discovery projects.

The role will involve building alliances with Discovery Oncology teams at the Boston and South San Francisco sites, championing new technologies, and interfacing with our global pharmacology network. The successful applicant will also have the skill sets to collaborate with teams in different functional areas (e.g., Bioinformatics, Discovery Chemistry, and Discovery Biologics) in a highly matrixed system and with external partners.

The successful candidate will:

  • Perform experiments using preclinical species to support the discovery and clinical development of novel Oncology compounds.
  • Manage external studies at CROs and academic collaborators including monitoring study execution and ensuring finalization of study reports within set timelines.
  • Partner and align with our global, network-wide organizational objectives, and ensuring that we remain at the forefront of drug discovery.
  • Foster a culture of innovation and continuous improvement within the QB/Pharmacology team, driving the development and adoption of new methodologies and technologies.
  • Ensure compliance with company established practices and procedures, including laboratory notebooks, computer files, quality and regulatory guidelines, and safety standards.
  • Education:

    • PhD in Oncology, Pharmacology, Biology, Pharmaceutical Sciences, Chemistry, Immunology, Biotechnology, Molecular and Cell Biology, or related STEM field with 5+ years of industry / biotech experience in Oncology drug discovery, or an MS with 7+ years of experience, or a BS with 10+ years of experience.

    Required Skills:

    • Experience using preclinical models to evaluate the in vivo pharmacology of novel modality-agnostic oncology drugs (small molecules, antibodies, ADCs, TCEs etc).
    • Experience at managing external studies at CROs and academic collaborators including monitoring study execution and ensuring finalization of study reports within set timelines.
    • Proven managerial/supervisory experience with a track record of training, developing talent, and mentoring team members in the field of Oncology/pharmacology and drug discovery.
    • Proficiency in complex problem-solving and the ability to influence strategy across organizational boundaries.
    • Strong skills in strategic thinking, effective communication, collaboration, balanced risk-taking, and a relentless pursuit of excellence.

    Required Skills:

    Immunoassays, Immunohistochemistry (IHC), Immunology, In Vivo Models, In Vivo Studies, Mass Spectrometry Imaging, Molecular Biology, Mouse Models, Multiplex Assays, Oncology, Pharmacodynamics, Pharmacokinetics, Pharmacology, Preclinical Research, Tumor Biology

    Preferred

    Skills:

    Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please  if you need an accommodation during the application or hiring process.

    As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

    For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

    EEOC Know Your Rights

    EEOC GINA Supplement

    The salary range for this role is $ - $. 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  (or via the Workday Jobs Hub if you are a current employee).

    Position Requirements
    10+ Years work experience
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