Scientist, Pharmacokinetics
Rahway, NJ - USA
Job Summary
Job Description
Role Overview
Our Company is a global biopharmaceutical leader with a diverse portfolio of prescription medicines oncology vaccines and animal health products.
We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69000 employees operating in more than 140 countries we offer state of the art laboratories plants and offices that are designed to Inspire our employees as we learn develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the worlds biggest investors in Research & Development.
Specific Responsibilities include:
Execute defined outsourcing activities for assigned studies or program components
Support CRO/vendor relationship management including meeting coordination documentation and timelines
Review proposals protocols test methods and bioanalytical reports for accuracy completeness and compliance
Contribute to inspection readiness through adherence to established processes and documentation practices
Support CRO onboarding contracting workflows and coordination with Research Procurement
Assist with preparation and participation in CRO site visits and performance reviews
Identify risks or performance concerns and escalate appropriately with proposed mitigation options
Participate in continuous improvement initiatives across outsourcing operations
Identify process inefficiencies or pain points and propose improvement ideas
Adopt and reinforce standardized processes tools templates and metrics
Support implementation of new workflows systems or operating models
Networking and partnership building with Subject Matter Experts (SMEs) to guide the science so our Companys quality expectations are achieved
Education Minimum Requirement
Bachelors degree in Biology Cell Biology Immunology Biochemistry or related field with 2 years of experience in immunoassay techniques including ligand binding assays cell-based functional and neutralization assays and/or molecular assays specializing in vaccines method development and validation or Masters degree
Required Experience and Skills
Experience in bioanalytical development and validation and/or quality control (QC) with knowledge of regulatory expectations for operating in a regulated clinical testing environment
Ability to manage defined project components with guidance
Strong organizational communication (oral and written) and teamwork skills
Familiarity with automated processes automated data workflows and/or AI-assisted tools in a scientific or data-driven environment with openness to expanding technical capabilities
Experience with one or more of the following techniques:
Ligand binding assays
Cell-based functional or neutralization assays
PCR/RT-PCR
Preferred Experience and Skills
2 years of experience working in a regulated assay environment and familiarity with FDA bioanalytical guidance requirements
Required Skills:
Assay Assay Development Bioanalysis Biochemical Analysis Biochemical Assays Biochemistry Cell Culture Techniques Clinical Judgment Data Analysis Data Visualization Detail-Oriented Ethical Compliance GMP Documentation Good Laboratory Practices (GLPs) Immunoassays Ligand Binding Assay Meeting Planning Operational Excellence Pharmacodynamics Pharmacotherapeutics Project ManagementPreferred Skills:
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 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:
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 anothers 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 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
$87300.00 - $137400.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees 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 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 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:
RegularRelocation:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
05/1/2026*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.
Required Experience:
IC
About Company
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more