Principal Scientist, Translational Clinical Biomarkers - Hematology/Oncology
$190.8k - $300.3kMerck Sharp & Dohme (MSD)
Job DescriptionWe are seeking an accomplished and highly motivated Principal Scientist to provide strategic and scientific biomarker leadership across programs within the Oncology and Hematology portfolios.This role will lead the design, execution, analysis, and communication of translational and clinical biomarker strategies across programs spanning early through late clinical development.The successful candidate will develop decision-centric biomarker strategies that integrate therapeutic mechanism, tumor or disease biology, pharmacodynamics, molecular heterogeneity, patient selection, response and resistance, dose and regimen selection, and clinical endpoints. Biomarker plans should focus on generating high-value, interpretable evidence that informs program decisions rather than data generation alone.Key Responsibilities* Develop and lead integrated biomarker strategies across oncology and hematology programs, in partnership with cross-functional development teams.* Translate disease biology and therapeutic mechanism into clear translational hypotheses and fit-for-purpose biomarker approaches.* Define how biomarkers can inform key development questions including proof of biology, target engagement, dose and regimen selection, patient selection, response assessment, resistance mechanisms, and go/no-go decisions.* Ensure biomarker strategies are focused and scalable, with clear linkage between the development question, proposed measurement, expected result, and potential action.* Serve as the biomarker representative on cross-functional program teams and provide strategic biomarker input to program-level decision making.* Partner closely with Discovery, Clinical Development, Quantitative Sciences, Regulatory, Data Science, Clinical Operations, Pathology, Diagnostics, and other functions to develop integrated translational strategies.* Lead interpretation of biomarker and clinical datasets and translate complex findings into clear, actionable recommendations.* Develop approaches to characterize disease heterogeneity, molecular drivers, treatment response, mechanisms of resistance, and biological determinants of clinical outcome.* Develop and evaluate patient-selection and precision-medicine strategies, including approaches based on genomic, transcriptomic, protein-expression, cellular, or other disease-specific biomarkers.* Apply circulating and tissue-based biomarker approaches, as appropriate, including ctDNA, minimal residual disease, molecular profiling, immunophenotyping, and pharmacodynamic biomarkers.* For hematologic malignancies, develop strategies incorporating disease-relevant measures such as molecular response, measurable residual disease, clonal evolution, mutational burden, lineage or cellular phenotype, and resistance-associated alterations, as appropriate to the program.* For solid tumors, develop strategies addressing target expression, tumor biology, molecular subtype, immune contexture, circulating biomarkers, mechanisms of response and resistance, and potential predictive biomarkers.* Evaluate emerging biomarker technologies and analytical approaches based on their ability to address meaningful development questions and influence program decisions.* Contribute to biomarker strategies supporting potential companion diagnostic or regulatory biomarker development, where appropriate.* Communicate biomarker strategies, results, risks, and recommendations clearly to cross-functional teams, governance groups, and key stakeholders.* Provide scientific guidance and mentorship to biomarker scientists and contribute to a collaborative, strategically focused biomarker organization.* Support publications, scientific presentations, external collaborations, and interactions with key external experts as appropriate.QualificationsEducationPh.D., M.D., or equivalent advanced scientific degree with relevant experience in oncology, hematology, translational medicine, biomarker science, drug development, or a related discipline.Required Experience and Skills* Significant experience developing and executing translational or clinical biomarker strategies in oncology or hematology drug development.* Strong scientific expertise in cancer biology, hematologic malignancies, translational oncology, or a related discipline.* Demonstrated ability to translate scientific hypotheses into biomarker strategies that inform clinical development decisions.* Strong understanding of the relationship between mechanism of action, disease biology, molecular heterogeneity, pharmacology, biomarkers, clinical endpoints, and development strategy.* Experience with one or more relevant biomarker modalities, such as NGS, ctDNA, MRD, immunohistochemistry, flow cytometry, gene-expression profiling, proteomics, or other molecular and cellular approaches.* Ability to lead cross-functional scientific work in a matrixed environment and influence without direct authority.* Strong analytical and problem-solving skills, including the ability to synthesize complex and multidimensional datasets into clear, decision-oriented conclusions.* Ability to prioritize high-value, decision-enabling biomarker work and distinguish it from lower-priority exploratory activities.* Excellent written and verbal communication skills and the ability to communicate scientific strategy to stakeholders.* Working knowledge of biostatistics, bioinformatics, quantitative sciences, and multidimensional biomarker data analysis.* Strategic mindset with a focus on scientific rigor, prioritization, scalability, and generation of actionable evidence.Preferred Experience and Skills* Experience supporting oncology or hematology programs across multiple stages of clinical development.* Experience with predictive, pharmacodynamic, prognostic, resistance, MRD, or precision-medicine biomarker strategies.* Experience integrating tissue, blood, molecular, and cellular biomarker data with clinical outcomes.* Experience supporting biomarker strategies for targeted therapies, immune-based therapies, antibody-drug conjugates, cell therapies, bispecifics, or other novel therapeutic modalities.* Familiarity with companion diagnostic development and associated regulatory considerations.* Experience working across multiple programs or disease areas.* Experience mentoring or providing scientific direction to other scientists.Required Skills: Biomarkers, Clinical Development, Clinical Research, Ethical Compliance, Immuno-Oncology, Mechanism of Action, Oncology, Patient Care, Pharmacodynamics, Protocol Development, Research Designs, Scientific Presentations, Scientific Writing, Strategic Thinking, Translational MedicinePreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here 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 RightsEEOC GINA SupplementWe are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State ActsThe salary range for this role is$190,800.00 - $300,300.00This 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 .You can apply for this role through (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 OrdinanceLos 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 OrdinanceSearch 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: RegularRelocation:DomesticVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:HybridShift:1st - DayValid Driving License:NoHazardous Material(s):N/AJob Posting End Date:10/9/2026*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. SummaryLocation: USA - Pennsylvania - North Wales (Upper Gwynedd); USA - Massachusetts - Boston (MA Parcel B Laboratory); USA - New Jersey - Rahway; USA - California - South San Francisco (Grand Ave)Type: Full time
$255.8k - $402.7k
...expanding your career. The Clinical Director (Principal Scientist) has primary... ...involving new or marketed Oncology medicines. Our company's... ...Evaluating pre-clinical and translational work for the purpose of... ...Eligible in Oncology (and/or Hematology)Prior specific...PrincipalFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$260.3k - $409.7k
...have an exciting opportunity for a physician-scientist to join our group as a Principal Scientist (Clinical Director) in Translational Medicine/Early Clinical Development in the... ...Phase 3 clinical trials.Development of biomarker strategies through cross-functional teams...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$260.3k - $409.7k
...Medicine is responsible for early clinical development of novel... ...and related conditions. The Principal Scientist (Clinical Director) must... ...background in basic and/or clinical translational research and a desire to... ...(Phase 2).Development of biomarker strategies through cross-...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$255.8k - $402.7k
Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities... ...May Be Responsible For:Evaluating pre-clinical and translational work for the purpose of generating the early clinical...PrincipalFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...Description Position Title: Principal Scientist, Early Development Center... ...Development (PSDD) organization translates molecules to medicines,... ..., packaging and release of clinical supplies for clinical... ...of prescription medicines, oncology, vaccines and animal health...PrincipalLocal areaRelocationVisa sponsorshipFlexible hoursShift work$190.8k - $300.3k
...and Development division, quantitative scientists, in partnership with other subject matter... ...global human healthStatisticians in the Clinical Safety Statistics (CSS) group develop strategic... ...and evaluation within CSS for key Oncology Therapeutic Area programs. Provide...PrincipalFull timeFor contractorsWork experience placementLocal areaFlexible hours- ...specialized capabilities from clinical through commercialization... ..., hepatic abnormalities, hematologic toxicity). Perform... ...Partner ~ Partner with Translational Medicine, Biomarkers, and Biostatistics to... ...certification in Hematology/Oncology (in U.S. clinic preferred...For contractorsRemote workWorldwideFlexible hours
$173.2k - $272.6k
...seeking an accomplished and highly motivated Principal Scientist to provide strategic and scientific biomarker leadership across programs within the... ..., execution, analysis, and communication of translational and clinical biomarker strategies across programs spanning...PrincipalFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$142.4k - $224.1k
...and Development division, quantitative scientists, in partnership with other subject matter... ...or large/complex late-stage drug/vaccine clinical development projects. Accountability... ...Modeling, FDA Submissions, Influencing Skills, Oncology, Presentation Delivery, Process...PrincipalFull timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$173.2k - $272.6k
Job DescriptionPrincipal Scientist Job Description: Our company's Pharmaceutical Sciences and Clinical Supply (PSCS) organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing...PrincipalFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$142.4k - $224.1k
...selection. In summary, our team enables the translation of preclinical candidates into non-... ...for the position of Associate Principal Scientist (R4) supporting the Biologics & Biopharmaceutics... ...Biotechnology, Chemical Engineering, Clinical Development, Design of Experiments (...PrincipalFull timeFor contractorsLocal areaFlexible hours$156.9k - $247k
Job DescriptionWe are seeking a Principal Scientist to join our Separations Sciences team, within... ...scales (µg to kg), enabling seamless translation from early-stage experimentation through... ...Analysis, Chromatographic Techniques, Clinical Judgment, Cross-Functional Teamwork,...PrincipalFull timeFor contractorsLocal areaFlexible hours$190.8k - $300.3k
...submissions that support global clinical development, product... ...Leaders, Compound Leaders, and scientists across NDS and/or Preclinical... ...chemistry, regulatory affairs, translational medicine, clinical... ...in immunology and/or immuno-oncology drug development. Experience...PrincipalFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ...SUMMARY Friday - Tuesday 9am-5pm Clinical , Hematology and Chemistry laboratory technologist... ...laboratory policies and procedures PRINCIPAL DUTIES AND RESPONSIBILITES... ...leading medical testing in Molecular Oncology, Hematology, Histopathology, and Chemistry...Immediate startShift work
$190.8k - $300.3k
...DescriptionJob Description:Our Scientists are our Inventors. Through... ...(BPR&D) as a Senior Principal Scientist.BPR&D within our Research... ...colleagues in Discovery, Pre-clinical, Early Development,... ...various strategic initiatives and translate strategies into implementation...PrincipalFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$109k - $174.8k
...Learn more at Position SummarySenior Scientist - Data (AI) Scientist, Translational Safety to join the Data, Data... ...modeling of biological (preclinical and clinical) and RWE data. The Senior... ...models that identify translational-biomarkers and flag compounds with high...Full timeWork at officeLocal areaImmediate start$142.4k - $224.1k
...and Development division, quantitative scientists, in partnership with other subject matter... ...or large/complex late-stage drug/vaccine clinical development projects. Accountability... ...Modeling, FDA Submissions, Influencing Skills, Oncology, Presentation Delivery, Process...PrincipalFull timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$142.4k - $224.1k
...implantation, and injection.The Associate Principal Scientist will provide end‑to‑end technical and... ...readiness to enable successful clinical introduction and commercialization.This... ...influence at all organizational levels, translating technical requirements into executable...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$173.2k - $272.6k
...company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state... ...Biostatistics, Statistical Programming, Data Management, Clinical Research, Regulatory, Observational Research, Clinical Safety,...PrincipalFull timeFor contractorsLocal areaFlexible hours$156.9k - $247k
...person will lead several Human Factors scientists to perform and manage human factors activities... ...Key Responsibilities and Activities:The Principal Scientist is responsible for managing a... ...management, formulation development, clinical, safety, regulatory, purchasing,...PrincipalFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...pipeline. We work closely with colleagues in Discovery, Pre-clinical and Early Development to rapidly develop manufacturing processes... ...motivated and experienced individual to join our team as a Principal Scientist. In this role, the successful candidate will lead cross-...PrincipalFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$142.4k - $224.1k
Job DescriptionAssociate Principal Scientist, Regulatory CMC - Biologics (R4)This Associate Principal Scientist position is equivalent to an... ...product supply.Lead authoring of clear, concise, and effective Clinical Trial Applications, Investigational New Drug Applications,...PrincipalFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours- ...Kelly Science and Clinical FSP is currently seeking a Sr. Clinical Scientist for a long-term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business...Full time
$173.2k - $272.6k
...pipeline. We work closely with colleagues in Discovery, Pre-clinical and Early Development to rapidly develop manufacturing processes... ...motivated and experienced individual to join our team as a Principal Scientist. In this role, the successful candidate will lead cross-...PrincipalFull timeFor contractorsLocal areaFlexible hours$156.9k - $247k
...person will lead several Human Factors scientists to perform and manage human factors activities... ...Key Responsibilities and Activities:The Principal Scientist is responsible for managing a... ...management, formulation development, clinical, safety, regulatory, purchasing,...PrincipalFull timeFor contractorsLocal areaFlexible hours$55 - $68 per hour
...Job Description Job Description Principal Scientist, NA Skin Health & Consumer Science Kelly Science and Clinical has an opening for a Principal Scientist f or an... ...by building deep consumer understanding and translating insights into actionable guidance through...PrincipalTemporary workWork experience placementLocal area$145.48k - $224.1k
...close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into... ...complex data preprocessing, filtering, and manipulation; Oncology franchise studies; applying oncology concepts; experience...PrincipalFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$145.48k - $224.1k
...Job Description DUTIES: ~ Support statistical programming activities for multiple and/or late-stage drug/vaccine clinical development projects. ~ Develop and execute statistical analysis and report deliverables (e.g., safety and efficacy analysis datasets, tables...PrincipalFull timeFor contractorsLocal areaRemote workWorldwideRelocationVisa sponsorshipFlexible hoursShift work$190.8k - $300.3k
...DescriptionThe Senior Director, Head of Clinical Development Learning &... ...Head of Clinical Science-Oncology and collaborate closely with... ...an expert, former Clinical Scientist with a minimum of 5 years of... ...adoption. Oversee the translation of new digital tools and analytics...Full timeFor contractorsLocal areaFlexible hours$210.4k - $331.1k
...DescriptionThe Senior Director, Clinical Data Intelligence & Medical... ...Heads of Clinical Science (Oncology and Non-Oncology), Clinical... ...needs of clinical scientists and clinical directors. The... ...improve current processes, translate user needs into clear requirements...Full timeFor contractorsLocal areaFlexible hours
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