Principal Scientist, Translational Medicine, Immunology
Company: Merck
Location: Rahway
Posted on: May 3, 2025
Job Description:
Job DescriptionBrief Description of PositionTranslational
Medicine is responsible for early clinical development of novel
therapeutics, working in close collaboration with Immunology
Discovery Sciences and late-stage Immunology Clinical Research. We
work with all therapeutic areas within our Research Division with
the role focused on Immunology. Clinical Directors must have a
strong background in basic and/or clinical translational research
and a desire to work collaboratively across different therapeutic
areas.Translational Medicine is specifically responsible for:
- Leadership of the early clinical development strategy for novel
therapy programs from Preclinical Candidate approval through
Clinical Pharmacology testing (Phase 1), and clinical
Proof-of-Concept (Phase 2).
- Development of biomarker strategies through cross-functional
teams that provide line-of-sight from First-in-Human studies
through clinical Proof-of-Concept. This includes Experimental
Medicine studies to establish and/or validate biomarker
platforms.
- Contributing to the identification of novel targets by
partnering with discovery research teams to bring a clinical
perspective into the earliest stages of target identification and
validation, and executing clinical studies to evaluate the
relevance of potential targets to human disease in order to justify
investment in clinical development programs.
- Development and execution of clinical pharmacology strategies
to support later stages of development from Proof-of-Concept (Phase
2) through worldwide marketing application.Success depends on the
integrity, knowledge, imagination, creativity, skill, diversity,
and teamwork of the people in the group. To this end, we strive to
create an environment of mutual respect, encouragement, and
teamwork. As part of the global team, you will collaborate with
talented and dedicated colleagues in Translational Medicine, as
well as Discovery Sciences and late-stage Clinical Research while
developing and expanding your career.Primary responsibilities
include the following:
- Key member of an early development team, providing leadership
in designing and executing early clinical development
strategy.
- Development and execution of early clinical strategy for novel
therapeutics including authoring initial clinical and biomarker
plans for Lead Optimization programs, early clinical development
plans for Preclinical Candidate molecules, and clinical
pharmacology studies for programs in Phases I through IV of
development.
- Development and execution of studies to validate clinical
platforms utilizing established and novel biomarkers, including
imaging, electrophysiological and behavioral responses to
interrogate biological activity in humans.
- Provide clinical expertise for identification and validation of
novel targets, including the design of preclinical and/or clinical
pharmacology experiments to validate targets and/or pathways.
- Safe and timely execution of Phase I studies; close
collaboration with internal and external clinical study support
staff and scientists (including discovery research, biostatistics,
drug metabolism, modeling and simulation, regulatory affairs, and
global clinical trials operations).
- Provide clinical pharmacology support for programs through the
worldwide marketing application filing including supportive
registration documents and presentations.
- Provide clear, timely communication and interpretation of study
results to therapeutic area governance, functional area experts and
development review committees.
- Contribute to assessment of internal and external opportunities
identified by Business Development and Licensing.
- Interface broadly with key functions including Discovery
Sciences, Preclinical Pharmacology, Pharmaceutical Sciences,
Toxicology, Translational Biomarkers, Translational Medicine
Operations, Translational Medicine-EU, Drug Metabolism/Modeling &
Simulation, Regulatory Affairs, and late-stage Clinical Research
throughout research sites around the world.Division/AreaClinical
ResearchExtent of Travel25%Qualifications, Skills &
ExperienceEducation:
- MD or MD/PhDRequired:
- Proven track record in clinical medicine or clinical research,
and background in biomedical research.
- Demonstrated record of scientific scholarship and achievement
including publications or presentations. The particular clinical or
scientific background is less important than having a track record
of excellence and a willingness to work collaboratively across
different therapeutic areas.
- Strong interpersonal, writing and presentation skills, as well
as the ability to function in a team environment are
essential.Preferred:
- Clinical Board Certification or Eligibility.
- Prior experience in translational research and/or early
clinical development preferred but not required.
- Proven track record in clinical care of patient populations or
management of clinical problem-solving.Employee
Status:RegularRelocation:VISA Sponsorship:Travel
Requirements:Flexible Work Arrangements:HybridShift:Valid Driving
License:Hazardous Material(s):Job Posting End Date:04/25/2025*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.Requisition
ID:R340751
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Keywords: Merck, Irvington , Principal Scientist, Translational Medicine, Immunology, Healthcare , Rahway, New Jersey
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