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Job Description
**Job Summary**
We are seeking a Research Associate to join our Insourcing Solutions team, located in Lexington, MA.
As the Research Associate, you conduct in vivo study work in rodents for multiple IS clients to support research programs. Collaborate with the veterinary staff to ensure the health and welfare of laboratory animals are maintained in compliance with guidelines and regulations.
Additional responsibilities include:
+ Able to perform and obtain competency/proficiency in the following techniques, at minimum:
+ Handle and restrain animals using appropriate procedures
+ Formulation and dosing calculations
+ Dosing and inoculation of test articles via basic techniques ( e.g., oral gavage, intravenous, subcutaneous, intraperitoneal, etc.)
+ Basic tissue (e.g.; spleen, liver, etc.) and blood collection (e.g., cardiac puncture, intravenous, etc.)
+ In-life monitoring of the study animals for body weights, clinical observations, tumor measurements, etc.
+ Monitors animal health and welfare while performing technical procedures.
+ Perform study preparation activities, including but not limited to, IACUC and study protocol review, collection tube labeling, and room setup.
+ Conduct laboratory procedures in compliance with approved IACUC protocols and study plans.
+ Operate and maintain lab equipment with guidance (e.g. Isoflurane machine, IVIS, Irradiator, and others).
+ Maintain accurate and up-to-date lab records/ documentation while assuring quality and data integrity.
+ Document experimental data as requested by clients in technical notebooks or approved electronic files.
+ Perform humane euthanasia in accordance with the Guide for Care and Use of Laboratory Animals, the AVMA Guide on Euthanasia, and under the direction of the attending veterinarian, or designee.
+ Report non-compliance or animal welfare concerns to the appropriate Animal Welfare Team member or IACUC office.
+ Collaborate with other personnel within and across teams/departments to facilitate completion of assignments.
+ Attend and participates in on-the-job and classroom training sessions, complete all assigned computer-based safety and professional development training by the pre-determined due dates.
+ Maintain effective communication with supervisor/ leadership and assists in reporting procedural deficiencies and issues.
+ Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed.
**Job Qualifications**
To qualify for this role, candidates must have one of the following combinations of education and experience.
Option 1:
Required: High School Diploma or GED AND either 1) a minimum of 2+ years of lab animal experience or 2) Certification from AALAS, at minimum the ALAT. Preferred: Basic in vivo technical skills.
Option 2:
Required: A.A./A.S. or B.A./B.S. in animal or laboratory (life) sciences or related discipline AND a minimum of 6-12 months lab animal experience. Preferred: Basic in vivo technical skills; ALAT certification.
The pay range for this position is $29 to $32 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
**About Insourcing Solutions**
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit
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Research Associate - Institute Community Health
Posted 8 days ago
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Job Description
**Requisition Number:** 12068
**Pay Range:** $23.25 - $35.06 per hour
**Location** : Commerce Place
**Category** : Research
**Department** : Institute Community Health
**Job Type** : Full ime
**Union Name** : Non Union
Work Schedule:Day
Length Of Shift(s) In Hours: 8
Shift Details:Monday-Friday from 9:00am-5:00pm
Hours/Week:40.00
Weekend Requirements:No
Holiday Requirements:No
On Call Requirements:No
Department Description
The Institute for Community Health (ICH) is a non-profit consulting organization that provides planning and assessment, participatory evaluation, applied research and data services to help local communities create sustainable health. The cornerstone of our mission is a commitment to community engagement in all aspects of the planning, evaluation and research processes, and a deep appreciation for the diverse experiences and values that communities contribute to health improvement. ICH has extensive experience working across sectors and with a broad array of organizations and institutions, including community-based organizations, city and state governments, hospitals and community health centers, and academic institutions. Our work spans a wide variety of topic areas, including chronic disease, health systems, youth development, health disparities, substance abuse, and mental health, among others.
Responsibilities:
The Research Associate is responsible for carrying out the day-to-day activities of evaluation, research, and planning and assessment projects, and conducting qualitative and quantitative data collection, analysis, and reporting.
Requirements:
+ Experience in research or evaluation, including developing data collection instruments and collecting and analyzing qualitative and quantitative data
+ Experience working with community organizations and diverse populations
+ Bachelor's or Master's degree in public health, public policy, sociology, psychology, or related field preferred
+ Be at ease interacting respectfully with community partners and community members
+ High attention to detail, good organizational skills and ability to multi-task
+ Ability to balance multiple projects and be flexible in day-to-day work tasks
+ Ability to work collaboratively with other ICH staff
+ Excellent written and oral communication skills
Please note that the final offer may vary within the listed Pay Range, based on a candidate's experience, skills, qualifications, and internal equity considerations.
In keeping with federal, state and local laws, Cambridge Health Alliance (CHA) policy forbids employees and associates to discriminate against anyone based on race, religion, color, gender, age, marital status, national origin, sexual orientation, gender identity, veteran status, disability or any other characteristic protected by law. We are committed to establishing and maintaining a workplace free of discrimination. We are fully committed to equal employment opportunity. We will not tolerate unlawful discrimination in the recruitment, hiring, termination, promotion, salary treatment or any other condition of employment or career development. Furthermore, we will not tolerate the use of discriminatory slurs, or other remarks, jokes or conduct, that in the judgment of CHA, encourage or permit an offensive or hostile work environment.
_Cambridge Health Alliance brings Care to the People - including your neighbors, friends and family. Our local hospitals and care centers serve our vibrant, diverse communities, and play an integral role in improving health. As passionate advocates for the underserved, we actively partner with our communities to take on challenging public health issues, and conduct important research to help reduce barriers to care. We believe that everyone deserves access to high quality, convenient health care. This is why our employees believe in where they work and why many build long, rewarding careers at CHA._
_Healthcare is changing rapidly. CHA has a strategic plan that charts a proactive course for our future. It is built on a vision of equity and excellence for everyone, every time. It also recognizes that our workforce is our most valuable asset and prioritizes competitive salaries, benefits and professional development opportunities for employees. The strategic plan is changing the way we provide care and improving the health and experience of our patients; we are looking for smart, committed, compassionate people who want to be part of making our vision of better health and equity a reality._
_At CHA, you can believe in where you work and go home every day knowing you made a difference. Join our team and help us bring Care to the People._
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Job Description
العودة to the job title not present, omitted for brevity Compensation:
$75K Salary + Bonus (All-In Compensation Target of $125K)
Start:Immediate
Description:Opportunity to conduct and analyze in-depth market research, and spearhead weekly publications to a network of 30,000+ industry contacts on behalf of AGC, the most active global technology mid‑market M&A investment bank. տեսակ aô. (continued in original paragraph)
Responsibilities:- Write, edit, and strategize content for whitepapers and related reports that cover the key trends and challenges in the technology market
- Build market maps and related lists that capture highly relevant software companies within a respective sector/space, create transaction screens to contextualize activity, and identify comps to benchmark valuations
- Manage a dynamic group of researchers across BDA, Operations, and Intern teams by developing effective project plans, providing daily instruction and feedback, and carefully monitoring work product
- Maintain proprietary databases of public and private software companies and synthesize market data into concise formats for Partner and client consumption, leveraging key findings to develop new content for whitepapers
- Further the firm’s private equity and venture capital relationships by tracking investment criteria, portfolio companies, and investment and exit activity
- Support AGC conference teams by identifying prospects to invite, preparing keynotes and other presentation materials, and attending conferences to facilitate meetings between companies and investors
- Develop and maintain standards, systems, templates and best practices to keep content cutting‑edge
- 2 years of experience preferred
- A motivated and tenacious individual with leadership skills and a passion to overcome any challenge
- Extremely organized, self‑motivated with effective communication skills (inter‑office and with clients) with a clear ability to establish, enforce, and meet deadlines
- Technology savvy and proficient in Microsoft Outlook, Word, Excel and PowerPoint (familiarity with PitchBook, 451 Research, SourceScrub, and Salesforce are a plus)
- Exemplary grammar, messaging, writing, and style
- Strong work ethic and personal integrity
- Passion for technology and keeping up‑to‑date on industry news and the latest M&A transactions
AGC Partners is a leading global technology investment bank that has advised on over 560 deals … (continued in original paragraph)
To Apply: Send your resume and cover letter to Matt Stumpf
Seniority Level:Associate
Employment type:Full‑time
Job function:Research, Analyst, and Information Technology
Industries:Investment Banking
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Job Description
Join to apply for the Senior Research Associate role at BioSpace
Join to apply for the Senior Research Associate role at BioSpace
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By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:
JOB LOCATION: Cambridge, MA
POSITION : Senior Research Associate
POSITION DESCRIPTION : Takeda Development Center Americas, Inc. is seeking a Senior Research Associate with the following duties: Provide a broad class of cell-based functional assay support to assess the functionality of Takeda’s lead antibodies, antibody-drug conjugates, and related modalities against their intended targets, in disease areas spanning oncology, gastrointestinal, central nervous system, and rare diseases; develop biological functional assays to characterize antibodies for drug candidates; support lab automation; analyze data, interpret results, and present findings to project teams; maintain accurate records. Less than 10% remote work allowed.
REQUIREMENTS: Master’s degree in Pharmaceuticals Sciences or related field plus 2 years of related experience. Prior experience must include: Develop bioassays using the MSD platform, with a proven track record of delivering optimized assay for phase 1 candidate Qc batch analysis; Work with primary cells/ tumor model for different cancer/disease markers; Hands-on experience with luciferase-based assay for reporter signals; Understanding of how to develop an assay, conduct optimization to validate the assay for screening and utilize this knowledge for developing any new assay for the incoming projects so that the assay is fit for use for Target of interest.
Full time. $93,000 to $155,800 per year. Competitive compensation and benefits.
Qualified applicants can apply at Please reference job #R . EOE
Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
Locations Boston, MA
Worker Type Employee
Worker Sub-Type Regular
Time Type Full time
- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Research, Analyst, and Information Technology
- Industries Internet News
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Cambridge, MA $156,000.00-$296,500.00 4 days ago
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Senior Principal Research Scientist, Physics-Based Methods Development Senior Director of Product Management, Research SolutionsGreater Boston $256,000.00-$352,500.00 3 weeks ago
ACADEMIC RESEARCHER or SENIOR ACADEMIC RESEARCHER, Global China Initiative, Global Development Policy Center Quantitative Investment Researcher (Assistant Vice President)Boston, MA $70,000.00-$100,000.00 2 weeks ago
Boston, MA $180,000.00-$240,000.00 6 days ago
Academic Researcher or Senior Academic Researcher, Global Development Policy Center Scientist, Syntein Purification & Physicochemical Properties Senior Experience Research Operations Specialist Academic Researcher or Senior Academic Researcher, Global Development Policy Center Senior Research Scientist - Astrophysics/Particle PhysicsWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Job Description
Join to apply for the Senior Research Associate role at Real
This range is provided by Real. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range$45.00/hr - $55.00/hr
Role SummaryOur client is seeking a highly motivated and detail-oriented Senior Research Associate to support our growing research and development efforts. The ideal candidate will have a strong background in immunoassay development and qualification, with hands‑on experience in ELISA and MSD-based assays. Experience handling and testing clinical patient samples, with a strong understanding of best practices for sample integrity and compliance. This role requires a collaborative team player who can interpret complex data sets, implement best practices, and maintain high standards of quality and documentation.
Key Responsibilities- Design, develop, and qualify immunoassays including ELISA and MSD platforms to support research and product development
- Experience with assay automation preferred but not required
- 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
- 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
- Bachelor's degree in Biology, Molecular Biology, Biochemistry, or a related scientific discipline with 3‑5 years of industry experience, or a 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 and draw meaningful conclusions
- 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
- Position requires at least 5 days of onsite in Boston
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
To find out more about Real, please visit
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Job Description
About The Opportunity
Northeastern University has established a Postdoctoral Researcher position dealing with cutting-edge research in the theoretical and applied aspects of resilient artificial intelligence (AI). The successful candidate will join Prof. Francesco Restuccia’s research team (website: in Boston, Massachusetts, and work on cutting-edge topics in resilient AI, including adversarial AI and out-of-distribution detection. The successful candidate will have a strong track record in top-tier AI publications, outstanding presentation and leadership skills.
ResponsibilitiesProvides scientific and technical leadership in the management, design, and conducting of the entire research program in resilient AI within Prof. Restuccia’s research group. Responsibilities include designing, developing, and establishing standards for the research to be conducted on topics related to resilient AI; publishing findings; obtaining new grants; developing project budget; interviewing, hiring, and managing all professional and technical staff; and supervising students.
Qualifications Mandatory- PhD in Computer Science or similar field;
- At least one (1) publication as first/second author in top-tier AI/ML venues (AAAI, ICML, ICLR, ICCV, ECCV, CVPR, WACV, NeurIPS, TNNLS) or evidence of strong research contributions in AI/ML;
- Excellent interpersonal, written, and verbal communication skills.
- Proven experience in resilient AI research, including adversarial AI and out-of-distribution detection;
- At least six (3) first/second author publications in top-tier AI venues (AAAI, ICML, ICLR, ICCV, ECCV, CVPR, WACV, NeurIPS, TNNLS) of which three (3) as first author;
- Demonstrated proposal writing experience;
- Demonstrated leadership skills.
Please submit through the website a (i) cover letter, (ii) a detailed curriculum vitae, (iii) three representative scientific publications, and (iv) the names and contact information of at least three references. References will only be sought for finalists. Applications submitted without this material will not be considered.
Position TypeResearch
Additional InformationNortheastern University considers factors such as candidate work experience, education and skills when extending an offer.
Northeastern has a comprehensive benefits package for benefit eligible employees. This includes medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement- as well as commuting & transportation. Visit for more information.
All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, religion, color, national origin, age, sex, sexual orientation, disability status, or any other characteristic protected by applicable law.
Compensation Grade/Pay Type108S
Expected Hiring Range$59,425.00 - $83,935.00
With the pay range(s) shown above, the starting salary will depend on several factors, which may include your education, experience, location, knowledge and expertise, and skills as well as a pay comparison to similarly-situated employees already in the role. Salary ranges are reviewed regularly and are subject to change.
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Job Description
Join to apply for the Senior Research Associate role at Tufts Medicine
1 day ago Be among the first 25 applicants
This role focuses on research and development of new products, innovation, and process improvements. It involves supporting the development of new products and innovation, including clinical research roles. Positions in this family perform basic, translational, and/or clinical research aimed at solving specific problems for an entity or community. The role is that of a professional individual contributor, potentially directing or managing processes and programs, with most of the time spent overseeing design, implementation, or delivery of processes, programs, and policies using specialized knowledge typically acquired through advanced education. It is a specialist level role, recognized as a subject matter expert, managing large projects or processes with limited oversight, resolving complex problems.
This position assists in research activities under supervision, working as part of the core staff to perform routine programmatic functions or research procedures with proper documentation. The role involves designing and performing research activities independently and collaboratively to achieve research objectives as directed by the Principal Investigator.
Minimum Qualifications:- Doctoral Degree OR Master’s Degree OR Bachelor’s Degree AND two (2) years of related experience.
- Five (5) years of experience in a research environment.
- Seven (7) years of research experience in multi-institutional observational studies and clinical trials.
- Develop and optimize project methods and protocols to meet research objectives.
- Interpret experimental data and unusual findings.
- Present research data summaries in group meetings.
- Perform research activities aligned with goals set by the Principal Investigator.
- Maintain detailed, organized, and clear research records and databases.
- Support investigators in developing research proposals and manuscripts.
- Manage day-to-day operations of research studies, including grant maintenance, budget review, and data collection.
- Supervise Research Assistants and Administrative Assistants.
- Organize complex data collection efforts and manage data files.
- Coordinate multiple research projects, delegating tasks and setting agendas.
- Conduct literature searches and participate in manuscript writing.
- Supervise interns and junior staff as needed.
- Assist in grant development and oversee database updates.
- Participate in data review and consult on future program directions.
- Largely sedentary role involving sitting, with movements like walking and reaching.
- Requires speaking, hearing, and communication skills.
- Ability to see and read computer displays and fine print.
- Manual dexterity for operating office equipment.
- Expertise in medical literature searching and retrieval.
- Proficiency in internet-based searching.
- Computer skills in Word, Excel, Access, and reference software like Endnote.
- High attention to detail and precision.
- Team participation and self-motivation.
Tufts Medicine is committed to diversity and inclusion, providing reasonable accommodations for individuals with disabilities. For accommodations, contact
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Job Description
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Contract Research Associate/Sr. Research Associate, In-Vivo Pharmacology (Must Have PO Dosing E[...]
Posted 6 days ago
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Job Description
Title: Contract Research Associate/Sr. Research Associate, In‑Vivo Pharmacology (Must Have PO Dosing Experience)
Hourly Rate: $35-$55/hour
Term: 6 Month Contract
Location: Downtown Boston (On‑Site Daily)
Job SummaryWe are seeking a highly motivated research associate to join our dynamic drug discovery team. This candidate will serve a critical role in executing in vivo pharmacokinetic (PK)/pharmacodynamic (PD)/efficacy studies in mouse tumor models for projects in early discovery to the pre‑IND stage. This individual will also work seamlessly with various biology functions to develop and run PD assays in the lab. This position is ideal for a talented, highly motivated and results‑driven individual who will thrive in a fast‑paced, innovative, start‑up environment.
Key Responsibilities- Conduct in vivo studies by providing dosing support and executing PK/PD/efficacy studies in mouse tumor models
- Maintain high‑quality, detailed experimental records within the ELN
- Use organizational and communication skills to effectively collaborate with colleagues across pharmacology and biology
- May require occasional weekend oversight of experiments
- BS in Biology or a related field
- A minimum of 2 years of relevant laboratory experience in industry
- Skilled in animal handling, tumor implant, dosing (PO/IV/SC/IP) and necropsy techniques
- Outstanding organizational, analytical and interpersonal skills
- Experienced with pipetting and cell culture
- Understanding of molecular biology techniques such as western blotting, qPCR, and other plate‑based assays and desire to learn to perform these assays
- Proficiency analyzing data with Excel, Prism and experience using an ELN system
- Experience with StudyLog software is a plus
- Experience with models of autoimmunity/inflammation is a plus
- Ability to multi‑task in a fast‑paced environment while maintaining the highest quality of experimental execution/quality
- Desire to contribute to teams working on challenging technical and scientific problems
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