Research Scientist

Job Title: Research Scientist

Location: Cambridge Crossing, MA

Duration: 12 Months

Pay Rate: $45.87 - $50.90/ hr on W2

100% onsite role

Work hours/schedule: M - F, typical work hours are 9:00am to 5:00pm

Parking Fee: Candidates must be agreeable with the $20/day parking fee at Cambridge Crossings.

Top 3 to 5 Skills:

Cell Culture

Drug combination screen

Molecular Biology

The Department is a key research and early development engine, responsible for the discovery and development of novel oncology therapeutics for patients. Centered at our state-of-the-art research sites in Cambridge and Seattle, scientists focus on novel targets and pathways for tumors that are refractory to current therapies. With a deep understanding of the causal human biology, we are able to leverage our multiple modality platforms to best match the modality to the mechanism and desired outcome. We are a fully integrated drug discovery through translational and early clinical development organization which exploits state-of-the-art in vitro, in vivo and ex-vivo models of Cancer biology and Immuno-oncology to identify and validate targets. We partner closely with colleagues in Translational Medicine, Informatics and Predictive Sciences and Early Clinical Development to generate biomarker and patient enrichment hypotheses to enable efficient decision making in early clinical trials. We are optimally positioned to complement the world-class translational expertise, biology and leading academic research centers in the area.

Our client site in Cambridge Crossing will help us continue to deliver on our mission, positioning the company and our scientists in the heart of a vibrant ecosystem of world-class science, innovation, and business opportunities.

Position Summary:

We are seeking an experienced individual with oncology discovery and/or translational expertise to join the Translational Research team at our client in Cambridge, MA. The qualified candidate will work closely with the research organization to support drug discovery programs by conducting experimental work in a translational setting, including developing and implementing cutting-edge technology and novel cellular, molecular, and biochemical assays in cancer research, and delivering data for Oncology TRC programs.

Detailed Position Responsibilities:

In the role as an Associate Scientist or Scientist within Oncology Translational Research, the ideal candidate will:

Design, optimize, and set up high-throughput screening cellular assays to characterize drug responses and combinations in various in vitro oncology models.

Conduct molecular, biochemical and related assays including qPCR, ELISA, Western blot, immunostaining and basic microscopy.

Develop biomarker, pharmacodynamic and target engagement assays.

Execute, troubleshoot and interpret scientific experiments with some supervision.

Effectively communicate and document experimental procedures, analyze results and data through study reports and internal meetings.

Collaborate with other team members in areas of responsibility.

Basic Qualifications:

Bachelors Degree with 3-5 years of academic and / or industry experience

Or

Masters Degree with 1-3 years of academic and / or industry experience

Preferred Qualifications:

BS or MS with at least 3 - 5 years of industry experience in cellular biology, oncology and molecular biology in the pharma or biotech setting may be considered.

Hands-on experience in conducting cancer cell line and primary cell culture, expansion and functional assays.

Experienced in the design and development of cell-based and molecular assays in a high-throughput manner.

Experience performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to western blot, flow cytometry, qPCR, MSD/ELISA, RNAi, CRISPR.

Proficiency in utilizing software such as Graph Pad, Microsoft office etc. for data analysis and figure generation is required.

Excellent organizational skills and ability to maintain accurate, detailed record-keeping of laboratory data.

Ability to summarize and interpret scientific data and communicate well with peers and supervisors.

This posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myer-Squibb .

The starting hourly compensation for this assignment is the following range ($45.87 - $50.90/ hr ). While the final, individual compensation and any available benefits will be determined by your employer of record ASK Staffing, Inc (and not BMS), factors that will be included in making the final determination may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location where the job is performed. The starting hourly compensation may be subject to change.

About ASK Consulting

ASK Consulting is an award-winning, woman-owned staffing and recruitment solutions provider with over three decades of industry experience. We specialize in connecting businesses of all sizes—across IT, healthcare, engineering, finance, and more—with top-tier professionals. Backed by a global network and personalized service approach, our team is dedicated to building meaningful partnerships that drive organizational success and empower job seekers to excel in their careers.

Benefits

ASK Consulting provides comprehensive, ACA-compliant health coverage, along with dental, vision, Short- and Long-Term disability for eligible employees. We also offer commuter benefits, a 401(k) plan with no matching, and a referral bonus program. In addition, ASK Consulting offers unpaid leave and paid sick leave as required by law.

Equal Opportunity Employer

ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.

California Applicant Notice

ASK Consulting is committed to complying with the California Privacy Rights Act (“CPRA”), effective January 1, 2023, as well as all relevant data privacy laws in the jurisdictions where we recruit and hire. To learn more, please review our Notice to California Job Applicants Regarding the Collection of Personal Information on our website. Applicants with disabilities may request this notice in an alternative format by contacting [email protected] .

Fair Chance Employment Notice

If you are selected for a position at, ASK Consulting, your offer is contingent upon successfully meeting several requirements, which may include a criminal background check. In accordance with all applicable federal, state, and local “Fair Chance” ordinances and laws—such as the Los Angeles County Fair Chance Ordinance (FCO) and the California Fair Chance Act (FCA)—we consider qualified applicants with arrest or conviction records. The background check will evaluate whether any criminal history could reasonably pose a direct, negative impact on job-related safety, security, trust, regulatory compliance, or overall suitability for the role. Findings that raise concerns may result in withdrawal of a conditional job offer.

To learn more about how ASK Consulting collects and uses personal information during the recruiting process, please review our Privacy Notice and CCPA Addendum . As part of our recruitment efforts, we may ask you to disclose various categories of personal information, including identifiers, professional details, commercial information, educational background, and other related data. ASK Consulting will use this information solely to facilitate the recruitment process.

This posting does not constitute an offer of employment. All applicants seeking positions in the United States must be legally authorized to work in the United States. Submitting intentionally false or fraudulent information in response to this posting may disqualify you from consideration. Any eventual offer of employment will be considered “at will,” regardless of the expected assignment duration.