Associate Research Scientist Job at Brandeis University (Waltham)

Research Associate

Ready to redefine what's possible in molecular diagnostics? Join a team of brill...

Location

United States , Menlo Park

Salary:

73920.00 - 84480.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

BS or MS in Molecular and Cell Biology, Microbiology, Biophysics, Biochemistry, or related field
1-2 years of research experience (either during BS/MS or afterwards)
Previous experience with standard molecular biology techniques (in particular, extensive experience with PCR, electrophoresis, DNA purifications)
An ability to quickly learn mathematical, analytical, and experimental concepts
High mathematical and statistical aptitude (e.g., you find GRE math section to be extremely easy)
Great attention to detail

Job Responsibility

Perform experiments and assays under the guidance of Senior Scientists
Learn analytical and computational methodologies and analyze the results under the guidance of Senior Scientists
Assist Senior Scientists in assay development
Keep accurate and meticulous records of experimental details and results
Prepare biological samples and reagents to accelerate the R&D process
Manage, organize, and support lab operations

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

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

Animal scientist

Animal Scientists research in the genetics, nutrition, reproduction, growth, and...

Location

United States , NC Triangle Area

Salary:

62645.00 USD / Year

Durham Technical Community College

Expiration Date

Until further notice

Requirements

Associate in Science (AS) degree
Transfer to a baccalaureate science degree at a four-year college or university
Courses in biology, chemistry, engineering, geology, mathematics, or physics

Job Responsibility

Research in the genetics, nutrition, reproduction, growth, and development of domestic farm animals

Quality Control Analyst

Quality Control Analyst (East Windsor, NJ) (Multiple Openings)

Location

United States , East Windsor

Salary:

Not provided

Novitium Pharma

Expiration Date

Until further notice

Requirements

Must have bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related besides 1 year exp. as Quality Control Analyst / Chemist / Analyst / Scientist / Research Associate / Microbiologist / Related

Job Responsibility

Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies
conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry
Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups

Regulatory Specialist

Regulatory Specialist (East Windsor, NJ) (Multiple Openings).

Location

United States , East Windsor

Salary:

Not provided

Novitium Pharma

Expiration Date

Until further notice

Requirements

Must have bachelors in Pharmaceutical sciences / biology / microbiology / chemistry / chemical / Regulatory Affairs / Related + 1 year exp. as Regulatory Specialist /Quality Control Analyst / Chemist / Analyst / Scientist/ Research Associate / Related

Job Responsibility

Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence) of different dosage forms (Tablet, Capsule, Liquid & Solutions)
responsible for filing the Post Approval Supplements like CBE-0, CBE-30 (Changes being effective in 30 days) and Prior Approval Supplements (PAS)
submitting dossiers electronically after the approval of initial product submissions (ANDA)
review of the leachable and extractable reports generated for the oral Liquid & Solution drug products

New

Senior Scientist, Research

The Senior Scientist, Research, with limited guidance from more experienced scie...

Location

United States , Madison

Salary:

109000.00 - 185000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position
or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 4 years of related experience in lieu of a Ph.D.
or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 6 years of related experience in lieu of Ph.D.
3+ years of industry or academia experience in biology and/or chemistry
2+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
Demonstrated proficiency in molecular biology and/or biochemical techniques
Demonstrated proficiency in the principles of molecular biology, biochemistry, next-generation sequencing (NGS), genomics, and/or protein research
Working knowledge of statistical and mathematical methods in biology/genetics
including, but not limited to, statistical software, such as JMP
Strong understanding of GMP, ISO, and Quality Systems

Job Responsibility

Provide leadership to a team of junior research associates and scientists
Independently develop, plan, and conduct advanced research experiments, identify problems and discrepancies, analyze results, and identify and address trends in study data
Analyze research/experimental data, interpret the results, and provide insights into the next steps
Utilize and apply methods or technologies effectively and provide ideas for new techniques, when appropriate
Provide technical input and develop research plans, experimental outlines, and design
Prepare and provide information and data for scientific abstracts, industry conferences, project meetings, or publication
Generate, document, and communicate development plans for critical aspects of a project
Prepare and approve detailed technical procedures, protocols, and reports
Evaluate impact of nonconforming data to product or process
Maintain lab notebook in a clear, complete, and consistent manner, following all legal, ISO, and QSR requirements

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 eligible

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Staff Scientist

The Staff Scientist will design, conduct, and document research projects; and te...

Location

United States , Los Angeles

Salary:

70304.00 - 116563.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

5 years of post-graduate relevant research
Ph.D.
3 years of postdoctoral fellowship training required
Knowledge and advanced research skills in biochemistry, microbiology, protein conjugation, and protein purification

Job Responsibility

Design, conduct, and document research projects
Teach research to research associates, postdoctoral fellows, and technicians
Participate in writing of manuscripts and grant applications

Associate Research Scientist

Brandeis University

Location:
United States , Waltham

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 26, 2026

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