Associate Scientist (Clinical Assay) Job at Pfizer (Pearl River)

Associate Scientist - Clinical Immunology

At Pfizer, our purpose is to deliver breakthroughs that transform patients' live...

Location

United States , Pearl River

Salary:

60200.00 - 97500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

BA/BS in Science with 0 - 2 years of relevant experience
Strong attention to detail
Ability to collaborate and work effectively in a team environment as well as independently
Proficiency in computer skills, including word processing, Excel, PowerPoint, and relevant scientific software
Experience in developing and troubleshooting bioassays designed to assess antibody functionality
Experience with mammalian cells and aseptic techniques

Job Responsibility

Conduct biofunctional immunological assays to support vaccine clinical development, adhering to Good Clinical Laboratory Practice (GCLP) requirements
Maintain a detailed inventory of freezer reagents, including controls, proficiency panels, toxins, and reference standards
Collect, analyze, and critically review clinical and nonclinical data to support assay development, sample analysis, troubleshooting, qualification, and other laboratory projects, and present progress to colleagues and senior management
Execute sample testing and analysis for toxicology and clinical trials, and provide critical review of resulting clinical and nonclinical data
Build team skills and collaborate effectively within the work group
Stay current on all departmental and corporate training
Organize work to meet deadlines and apply technical skills
Follow procedures for assigned tasks and seek guidance when necessary

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary
Relocation assistance may be available

Fulltime

Associate Scientist, Translational Medicine

This role is located in Center City, Philadelphia and is primarily a lab-focused...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

MS degree in Biology or Bioengineering (or related field) with 2+ years of experience, or Bachelor's degree with 4+ years of experience in the biotechnology industry required
Proficiency in flow cytometry and flow cytometry data analysis (using FlowJo or equivalent software) is required
General lab skills, including aseptic techniques and human tissue handling required
Must be highly organized and able to work independently in a fast-paced environment
Must be able to clearly communicate in writing, must have a desire to be part of a growing organization that uses cutting-edge science
A high level of flexibility to support various other activities and the ability to learn new techniques outside of existing field of expertise
Strong team orientation and passion for continuous self-development

Job Responsibility

Perform and support the development of laboratory assays on clinical (and potentially pre-clinical) samples to generate translational data that informs safety, biological activity, and therapeutic impact of rese-cel
Manage clinical sample processing, accessioning, tracking, and lifecycle documentation with careful attention to metadata and data integrity
Maintain accurate, GDP-compliant experimental records using electronic laboratory notebooks (ELN) and sample management systems
Document all procedures and experimental parameters within our ELN and follow up with Quality Control/Assurance for review. Address and document any QA concerns and participate in root-cause assessments and CAPAs if necessary
Contribute to assay development, qualification, and validation efforts and assist in the preparation of related SOPs
Manage multiple internal projects and collaborate cross-functionally with Translational, Pre-clinical, and Analytical Sciences teams, as well as external partners
Perform laboratory activities in accordance with GLP/cGLP standards, company safety policies, and SOPs, including general maintenance of laboratory space
Other related duties, as assigned

What we offer

health and retirement, PTO, and stock option plans

Medical Laboratory Scientist II - Chemistry

Join a team that’s setting the standard for safety and quality. Every day as a Q...

Location

United States , Royal Oak

Salary:

Not provided

Quest Diagnostics

Expiration Date

Until further notice

Requirements

One (1) year full-time experience or training (high complexity testing) in a clinical laboratory setting
BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States-educated candidates must provide a detailed original transcript
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
Communication skills necessary to handle telephone inquiries from clients
Ability to deal with client information in a confidential manner
Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems

Job Responsibility

Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified
Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department
Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Ensure reagents/test kits have received dates, expiration dates and if applicable opened dates
Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test
Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures
Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness®
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 "MyDay" off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Histology Research Associate II

We are looking for an outstanding individual to join its Cell Biology and Applic...

Location

United States , Pleasanton

Salary:

38.00 - 48.00 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

BS/MS in Histology or similar
4 years of hands-on tissue biology and histology experience in an academic or industrial setting
Experience with provisioning or processing animal models and human clinical samples (tissue, biopsies, fresh frozen, fixed frozen, FFPE)
Experience with tissue sectioning: cryostat, microtome and paraffin embedding
Experience with immunostaining (IHC), in situ hybridization (ISH) and histology
Meticulous attention to detail and strong record-keeping skills
Desire to be part of a rapidly evolving organization, which requires flexibility and a willingness to take initiative, and learn new techniques and concepts
Committed to total customer satisfaction with outstanding interpersonal skills and professionalism

Job Responsibility

Assist in the implementation and optimization of electronic sample and reagent inventory management systems
Acquire, and maintain an inventory of relevant biological and clinical tissue samples, spanning from fresh mouse tissue to preserved human tumor biopsies
Assist in the screening of tissues for quality, composition, and biological significance
Assist in the development and optimization of sample preparation procedures/protocols for tissue and single cell genomic assays
Prepare and provide slides containing tissue sections to multiple product development teams, which includes responsibility for adhering to a tight schedule while maintaining exceptional quality
Advise and assist R&D scientists with histology experiments and methods
Assist in training other research associates, technicians, and scientists as required
Maintain cooperative, professional, and positive attitude when interacting with others internally and externally

What we offer

Comprehensive health benefit program
Generous time off
Family friendly policies like parental leave
Competitive easy-to-use benefits that promote wellbeing

Parttime

Research Associate II (Pre-clinical)

The Research Associate II (Pre-clinical) supports laboratory research experiment...

Location

United States , Rockville

Salary:

55000.00 - 65000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Master’s degree in a relevant scientific discipline (e.g., biology, chemistry, biomedical engineering) required
4–6 years' experience in laboratory research
Ability to exercise independent judgment in fast-paced research environments with strict deadlines
Ability to multi-task
Demonstrated competence in oral and written communication
Must be organized, attentive to detail, and possess a positive and professional demeanor
Must possess eligibility to work in the U.S. Visa sponsorship not provided.

Job Responsibility

Analyze and interpret scientific data
Lead the development of technical documentation
Support the training of junior scientific staff
Effectively communicate results to a broad range of experts and stakeholders
Execute research studies (under the direction of the project's Principal Investigator or Research Scientist), manage study documentation, and prepare progress reports
Interact and communicate effectively with Principal Investigator, other site personnel, and The Geneva Foundation personnel
Procure supplies and equipment as authorized per research budget guidelines
Assist with interim and annual reports
Actively participate in regular team meetings
Complete required and applicable research training needed to complete research

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Coverage is provided for employees and family members including domestic partners
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year

Fulltime

Scientific Associate Director - Pharmacokinetics and Drug Metabolism

In this vital and exciting role, you will oversee Pharmacokinetics and Drug Meta...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees and 12+ years of experience in the Biotechnology/Pharmaceutical Industry
Solid technical experience with the application of SM in vitro/in vivo ADME and pharmacokinetics fundamentals to drug discovery projects
Ability to drive the progression of SM discovery and development within project teams
Expertise with in vitro ADME, in vivo ADME, PK/PD etc
Experience in supporting preclinical components of regulatory documentations
Excellent interpersonal, technical, and communication skills
Past experience as a laboratory scientist in a pharma or biotech environment
Excellent written and oral communication skills, attention to detail and accuracy, and interpersonal skills
Record of scientific contributions through peer-reviewed articles and external presentations

Job Responsibility

Lead/mentor a team of scientists involved in ADME characterization of small molecules
Directly responsible for leading a team of scientists involved in undertaking mechanistic in vitro ADME assays
Develop/implement novel tools to efficiently support mechanistic ADME work
Oversee activities/establish workflows for small molecule bioanalytical and ADME screening teams
Serving as a subject matter expert of small molecule ADME to support the programs and recommend strategies to PKDM project team representatives to reduce/mitigate risks due to metabolism
Collaborate with scientists across our PKDM scientific community
Leveraging specialized ADME/PK skills such as in vitro ADME, in vivo ADME, biotransformation, PK/PD, to impact project progression and decision-making
Contributing to the analysis of pre-clinical ADME and PK data for IND and NDA filings and documenting these analyses in appropriate reports
Building close relationships with partner functions

Manager, Process Development and Automation

The Manager, Process Development and Automation provides leadership support to t...

Location

United States , Redwood City

Salary:

124000.00 - 200000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Engineering, Technology, Molecular Biology, Clinical Laboratory science, Chemical, biological, Electronics, or related field and 2 years’ experience as outlined in the essential duties
or Associates Degree in a Microbiology field or Engineering Science and 4 years’ experience as outlined in the essential duties in lieu of Bachelor's degree
2+ years in a role with progressively increasing responsibilities such as laboratory management, quality and control, lead technologist, or technical specialist
8+ years’ experience in process development, laboratory automation, service engineering, laboratory setting, or related industry as outlined in the essential duties
Successful track record of leading projects holistically from inception to successful implementation with cross-functional participation in a matrixed environment
Proficient in computer aided design software (SolidWorks) or statistical analysis programs (JMP), Microsoft Office Word, Excel, PowerPoint, and similar software
Working knowledge of regulatory requirements to make sure the laboratory is in compliance with all applicable laws and regulations, including applicable CLIA, CAP, California, New York (CLEP), and other requirements
Experience in the design, development, and implementation of solutions comprised of integrated automated and manual workflows, including software components in a highly regulated environment (ISO 13485 or 21 CFR Part 820, or cGMP using 21 CFR Part 210, 21 CFR Part 211)
Understanding and application of user requirements, system requirements, risk assessments, trace matrices, FMEA, etc. translating into a successful track record in understanding complex end-user applications, collecting and clearly documenting end-user needs, and translating those into clear, concise, and testable requirements
1+ years in a leadership role with staff and team accountability

Job Responsibility

Provide leadership on best practices for the development of processes and products in a regulated environment
Lead the team in continuous improvement projects and support other areas’ needs dependent on demand
Coach, mentor, and raise the team's ability to deliver and exceed expectations while creating opportunities for team member development
Consistent demonstration of exceptional leadership qualities
Effectively manage, support, and guide your team
Serve as a resource for employees by sharing and knowledge transfer of best practices for experiment design and execution
Ensure that any incoming support requests from outside of the normal channels are properly routed
Ensure that assigned support requests from cross-functional project teams or business units are being actively addressed
Assist and coordinate training methodology and training documentation in conjunction with other leadership
Provide mentoring and technical guidance to PDA engineers and scientists

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Reagent Development Scientist II

Client Biosciences is a world leader in bringing innovative diagnostic and resea...

Location

United States , San Jose

Salary:

28.00 - 32.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience with bench work
BS degree in Biology with Immunology as one of the subjects
analytical thinking and experience in MS Office
Experience in writing protocols, reports, and manufacturing documentation such as work instructions, SOPs, and manufacturing specifications
Experienced in bench-testing and has effective analytical and problem-solving skills
M.S. in Biology, Immunology, Biomedical engineering and other Biological majors
Knowledge of or demonstrated interest in immunology, hematology and/or clinical chemistry in the clinical, research and pharmaceutical environment
Lab skills, including pipetting, working with blood, cells or other sample types
Knowledge of general laboratory safety, GMP’s, and associated regulatory requirements
Minimum B.S. degree in Biology, Immunology, Biomedical engineering and other Biological majors

Job Responsibility

hands-on laboratory testing
basic flow cytometry workflows to assist in new assays and reagents development
preparation of biological samples
analysis of flow cytometry data
preparation of documentation
test method development/process validation studies
provide support for technology transfer of products and processes from R&D into operations
performing work under supervision of a project lead who will define deliverables
participate in project team meetings
be responsible for documenting and presenting findings

Fulltime

Associate Scientist (Clinical Assay)

Pfizer

Location:
United States , Pearl River

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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