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Senior Scientist, Quantitative Pharmacology and Pharmacometrics at Merck USA in Rahway, NJ

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Description

Requisition ID: PHA001398

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.


Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 


Senior scientists in Quantitative Pharmacology and Pharmacometrics (QP2) apply quantitative approaches to develop and implement translational PK/PD strategies, characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics, and inform dose selection and go/no-go decisions. Senior Scientists work in collaborative teams with more experienced scientists, and are expected to have or develop expertise in one or more areas necessary to performing primary responsibilities including:

  • Being or supporting the lead representative for QP2 on drug/vaccine development teams
  • Data management and analysis 
  • Framing critical drug development questions for optimizing model-based development
  • Developing and executing translational PK/PD approaches, population pharmacokinetic models, exposure-response and stratification biomarker models, quantitative system pharmacology (QSP) and disease progression models, clinical trial design via outcome/enrollment modeling and simulation, comparator modeling, absorption/biopharmaceutical modeling, clinical utility index modeling, and other model-based analyses. 

Senior Scientists are expected to develop a comprehensive understanding of global regulatory expectations for small molecules, biologics, and/or vaccines, including support for regulatory documents (INDs, CSRs, CTDs), and agency interactions. The Senior Scientist is a proficient modeler, is able to develop a strong, integrated understanding of the strategic elements of drug discovery and development, and contributes to or leads the combined efforts of QP2 and the wider Department of Pharmacokinetics, Pharmacodynamics and Drug Metabolism (PPDM). 


Senior Scientists begin to develop leadership skills in areas such as mentoring, managing a program (while collaborating with QP2 Program Lead), project, or initiative. In addition to the responsibilities outlined above, Senior Scientists demonstrate good communication skills, collaborating within QP2 and with other functional areas, as well as with external vendors and partners, creating an aligned, quantitative framework to impact decisions of drug development teams. 

Qualifications

Education:

  • Master or equivalent degree with at least four years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development or academia.

Required:

  • Ph.D. or equivalent degree - OR- a PharmD or equivalent degree with at least two years of experience or an educational background in biopharmaceutics, pharmaceutical sciences, pharmacometrics, mathematics, statistics/ biostatistics, computational biology/chemistry, chemical/biomedical engineering, or a related field.
  • Proficiency in R, Matlab, SAS, or other similar programing language

Preferred:

  • Experience in performing population PK / PKPD and non-compartmental analyses
  • Experience with standard pharmacometric software (e.g. NONMEM, Monolix, Phoenix, etc.)
  • Skills in experimental design, mathematical problem solving, critical data analysis/interpretation, and statistics
  • Scientific understanding of biopharmaceutical and ADME properties 
  • Proficiency in written and verbal communication, interdisciplinary collaboration, and problem scoping and planning

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 

 

If you need an accommodation for the application process please email us at staffingaadar@merck.com.

  

Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 


ACoP



Job: Pharmacokinetics/Drug Metab
Other Locations:
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck

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