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Merck
Job DescriptionThe Quantitative Pharmacology and Pharmacometrics (QP2) department of our company's Research Laboratories in Rahway, NJ is seeking a collaborative Operations Scientist to join our QP2 O...
Jul 8, 2025
Rahway, NJ
Merck
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Jul 1, 2025
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Merck
Job DescriptionThe West Point Technical Operations Laboratory Process Support group within our Company Manufacturing Division is responsible for supporting all commercial vaccines with best in class l...
Jul 1, 2025
West Point, PA
Merck
Job DescriptionThe Data-Rich Measurements (DRM) Group within Analytical R&D Enabling Capabilities organization is seeking a highly motivated individual as a Principal Scientist at its West Point, Penn...
Jun 20, 2025
West Point, PA
Merck
Job DescriptionThe Data-Rich Measurements (DRM) Group within Analytical R&D Enabling Capabilities organization is seeking a highly motivated individual as a Principal Scientist at its West Point, Penn...
Jun 20, 2025
West Point, PA
Quantitative Pharmacology & Pharmacometrics Operations Specialist
Rahway, NJ
Jul 8, 2025
Full-time

Job Description

The Quantitative Pharmacology and Pharmacometrics (QP2) department of our company's Research Laboratories in Rahway, NJ is seeking a collaborative Operations Scientist to join our QP2 Operations Team.

Responsibilities:

The QP2 Operations Scientist will work with QP2 scientists and cross-functional partners to advance the pipeline of novel therapeutic agents at our Company. QP2 Operations Scientists will enable tactical, logistical and operational elements of pertinent workflows, including but not limited to those in support of data needed for QP2 modeling, support of filings, and management of regulated document workflows. The Operations Scientist will develop a deep understanding of how to enable QP2 deliverables with a focus on strategically solving tough operational and scientific challenges, streamlining end-to-end process, and improving operational efficiency. More specifically, an Operations Scientist will work with QP2 scientists and key partner functions (such as bioanalytical sciences, data management, statistics/statistical programming, and external vendors) to:

  • Enable smooth functioning and continuous improvement of QP2 involvement in clinical trials, including troubleshooting to resolve clinical study data issues.

  • Ensure QP2 data requirements are integrated into evolving clinical data systems.

  • Support QP2 needs for clinical trial operations, dataset creation, analyses (including conducting noncompartmental analysis) and reporting.

  • Simultaneously manage timelines of multiple clinical studies, QP2 deliverables and document reviews.

  • Gain expert level familiarity with regulatory publishing and take primary responsibility for publishing and editorial filing readiness of modeling and simulation reports for filings.

The selected candidate will be expected to operate with an enterprise mindset, be comfortable operating in ambiguous situations and with independence.

Education Requirement:

A MS, PharmD or equivalent degree - OR- a BS or equivalent degree with at least two years of experience, where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development or academia.

Skills:

Required:

  • An educational background in quantitative sciences, including but not limited to pharmaceutical sciences, pharmacy, pharmacometrics, mathematics, statistics/ biostatistics, computational biology/chemistry, chemical/biomedical engineering or public health.

  • Excellent written/verbal communication and interpersonal skills with a proven ability to collaborate with individuals across multiple different areas of expertise.

  • Organization skills, strong attention to detail, an operations-oriented mindset, and a propensity for troubleshooting complex issues.

  • Proven ability to work on multiple projects at the same time and manage timelines/deliverables appropriately.

Preferred:

  • Background in health or pharmaceutical sciences.

  • Demonstrated leadership experience, with an ability to work through ambiguous situations, and a team-oriented enterprise mindset focused on identifying efficiencies and driving innovative solutions.

  • Knowledge of or experience with clinical trial conduct, trial operations, clinical databases and data standards (e.g CDISC, SDTM and ADaM).

  • Experience implementing noncompartmental analysis (NCA) using PK software (e.g. Phoenix), statistical software (e.g. SAS), or other pharmacometric analyses via NONMEM, Monolix, R, etc.

  • Proficiency utilizing Microsoft Office suite, in particular Microsoft Excel.

This is a unique opportunity to advance your career while learning the fascinating world of pharmaceutical R&D in one of the world's most research-intensive biopharmaceutical companies.

Your role at our Company 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 our Company, we're inventing for life.

Current Employees apply HERE

Current Contingent Workers apply HERE

US 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 Rights

EEOC GINA Supplement

We 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 Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote".

The salary range for this role is

$104,200.00 - $163,900.00

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):


Required Skills:

CDISC ADaM, Collaboration, Communication, Cross-Functional Teamwork, Data Analysis, Data Engineering, Data Science, Data Visualization, Pharmaceutical Development, Phoenix WinNonlin, Stakeholder Relationship Management, Study Data Tabulation Model (SDTM)


Preferred Skills:

Data Modeling, NONMEM, Pharmacometrics, R-Studio

Job Posting End Date:

07/14/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe 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:R355512

PDN-9f56a47b-0dc2-4a07-8690-f42168a11bc9
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Quantitative Pharmacology & Pharmacometrics Operations Specialist
Merck
Rahway, NJ
Jul 8, 2025
Full-time
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