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

New

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

Staff Scientist I

We are seeking a candidate who can bring experience of clinical flow cytometry w...

Location

United States , San Diego

Salary:

124700.00 - 205800.00 USD / Year

BD

Expiration Date

Until further notice

Requirements

Minimum Master’s degree or Ph.D. degree in biological science and a combination of education and experience in product development
Minimum 5 years of demonstrated experience in R&D or clinical/research laboratory environment
Experience in IVD product development is required
Strong, proven product development knowledge of processes, measures, etc. (phase gated development systems)
Knowledge of biostatistical methods and data analysis experience is required
Proven experience of working in cross-functional product development teams

Job Responsibility

Work with team members and lead collaborations across teams on crafting experimental approaches for new reagent and assay development
Maintain strong understanding of innovative science and technology development in the industry
Deliver clinical projects on schedule and within specification
Work with leadership team members and product development teams to improve time to market by reducing product development life cycle and improving the product development process
Prepare technical reports, summaries, protocols, and analyses of R&D projects
Work on issues where analysis of situation or data requires review of relevant factors
Exercise judgement within defined procedures and policies to determine appropriate action
Effectively coordinate with other functional areas associated with the R&D activities
Assure compliance with all local, state, federal, and BD policies/ procedures regulations associated with quality, regulatory, safety, etc.

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

Senior Research Associate, Preclinical and Clinical Biomarkers

The Department of Research and Translational Medicine is seeking a highly motiva...

Location

United States , Boston

Salary:

95000.00 - 110000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Biology, Molecular Biology, Biochemistry, or a related scientific discipline with 3–5 years of industry experience
Master’s degree with at least 2 years of relevant experience
Demonstrated expertise in immunoassay development and qualification, specifically ELISA and MSD
Strong analytical skills with the ability to interpret complex data
Experience implementing quality control measures and maintaining scientific documentation
Excellent communication and organizational skills
Ability to work independently and as part of a collaborative team in a fast-paced environment
Ability and willingness to travel including a minimum of 2 times per year for company-wide meeting
Ability to work onsite up to 5 days per week in the Apogee lab located in Boston, MA

Job Responsibility

Design, develop, and qualify immunoassays including ELISA and MSD platforms to support research and product development
Analyze and interpret complex biological data sets with precision and scientific rigor
Apply best practices to minimize assay variability and ensure reproducibility
Maintain detailed and accurate records of experimental procedures and results in accordance with quality control standards
Maintain the inventory of samples and associated paperwork according to our operating procedures
Assists with identifying needs and sourcing of reagents, samples, and other critical materials
Collaborate cross-functionally with other scientists and departments to support project goals
Contribute to troubleshooting and optimization of assay protocols
Ensure compliance with internal SOPs and regulatory guidelines

What we offer

Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Intern, Cytometry Shared Resource Lab

The BioMarin Summer Internship Program will enable students to gain valuable exp...

Location

United States , San Rafael

Salary:

24.00 - 32.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Undergraduate or Masters Candidate pursuing a degree in biochemistry, cell biology or equivalent, with an interest in a laboratory career preferred
Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
Must be available to work full-time, 40 hours a week
Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles
Required Coursework: Molecular Biology and Molecular Biology Laboratory or equivalent courses
Cell Biology or Molecular Immunology or equivalent courses
Cell Biology Laboratory or Molecular Immunology Laboratory or equivalent courses

Job Responsibility

Working with the Lead Scientist and Research Associates in the Cytometry Core within the Center of Technology
Gain knowledge of how flow cytometry, high content imaging and cell sorting are used in a biotechnology environment to support research, bioanalysis, and clinical work
Gain knowledge in how to operate a flow cytometer, high content imager and cell sorter
Receive training in a typical flow cytometry assay including complex options for data analysis
Gain experience in a Shared Resource Laboratory (SRL or Core Lab) touching many parts of the drug discovery process

What we offer

Apply skills and knowledge learned in the classroom to on-the-job experiences
Comprehensive, value-added project(s)
Work in teams and with colleagues in a professional environment
Develop skills specific to your major
Opportunities for professional development by building relationships and learning about other parts of the business
Participate in company all hands meetings, monthly community lunches
Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
Access to Employee Resource Groups

Fulltime

New

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

New

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

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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