536 Results for

Clinical Scientist Jobs in Cambridge, MA

Jobs

New!

Boston, MA4 days ago

$237,200–$372,790 Per Year

Assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with TPNA/TPEU/TPC. These responsibilities include leadership roles in meetings with the regulatory organizations or key opinion leaders, establishment of strategy for assigned compounds, and the direction of clinical scientists involved in developing documents required to outline the Company positions on research programs or regulatory applications (e.g.

New!

Cambridge, MA3 days ago

Remote

$237,200–$372,790 Per Year

Assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with GPLS & Business Units. These responsibilities include leadership roles in meetings with the regulatory organizations or key opinion leaders, establishment of strategy for assigned compounds, and the direction of clinical scientists involved in developing documents required to outline the Company positions on research programs or regulatory applications (e.g.

New!

Cambridge, MA4 days ago

$198,500–$311,850 Per Year

Provides leadership in meetings and negotiations with key opinion leaders, establishment of strategy for assigned compounds, and the direction of clinical scientists involved in developing documents required to outline the Company positions on research programs or regulatory applications (e.g. Contributes to the development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities, interacts with upper management of potential partner/acquisition companies during DD visits and alliance negotiations and represents clinical science on internal assessment teams.

New!

Boston, MAToday

$116,000–$182,270 Per Year

See Takeda Pharmaceutical Terms of Use at https://www.takeda.com/terms-of-use/ and Privacy Policy at https://www.takeda.com/privacy-notice/ and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.

New!

Easton, MAToday

Click to apply or send a resume directly to Marissa at marissak@ka-recruiting.com or call 617-746-2748. The role involves conducting laboratory tests to aid in patient diagnosis and treatment.

New!

Bridgewater, MAToday

Click to apply or send a resume directly to Marissa at marissak@ka-recruiting.com or call 617-746-2748. The role involves conducting laboratory tests to aid in patient diagnosis and treatment.

New!

Quincy, MAToday

This award winning hospital offers comprehensive services including (but not limited to) primary care, women's health, urgent care, and diagnostic care. Job DescriptionMedical Laboratory Scientist OR MT OR Medical Laboratory Technician at a not-for-profit hospital located in Southeastern Massachusetts!

New!

Boston, MA1 day ago

Key Responsibilities: Performing a variety of moderate and highly complex and diagnostic laboratory testing under general supervision in the laboratory. Performing regularly scheduled quality control, preventative maintenance, and calibration of equipment according to laboratory guidelines.

New!

Boston, MAToday

New!

Boston, MA1 day ago

New!

Boston, MA1 day ago

New!

Boston, MAToday

$154,400–$242,550 Per Year

Advanced knowledge of pharmaceutical industry, overall drug development process with expertise in the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance, digital strategy, library sciences and data architecture/governance) bring their expertise to our global program teams and reimagine our disciplines.

New!

Abington, MAToday

Description: - Performs a variety of routine and specialized diagnostic tests and/or operational support functions as assigned in Blood Bank, Chemistry, Hematology, and Microbiology. - Community-based, award-winning, non-profit healthcare organization that provides a full range of clinical services.

New!

Cumberland, RIToday

For consideration, applicants must have either a Bachelor's Degree in Medical Technology/MLS and/or an AS Degree in Medical Laboratory Science/Medical Laboratory Technician AND ASCP Certification as a MT/MLS, M/SM or MLT. Job DescriptionNEW Microbiology/Molecular Medical Technologist OR MLS OR MLT Opening at a full service clinical laboratory in Rhode Island!

New!

Foxborough, MAToday

The ideal candidate will perform routine laboratory tests, prepare specimens, and ensure accurate results in a fast-paced environment. Job DescriptionApply for this position as a Generalist Medical Technologist / Medical Laboratory Technician with a top healthcare facility in Foxboro, Massachusetts for permanent hire.

New!

Boston, MAToday

With a quick phone call, I can get a better idea of your background and begin a confidential search for positions that match what you are looking for. I have over 900 clients in the United States, so I am confident I can find your next full time position!

New!

Attleboro, MAToday

For consideration, applicants must have either a Bachelor's Degree in Medical Technology/MLS and/or an AS Degree in Medical Laboratory Science/Medical Laboratory Technician AND ASCP Certification (or equivalent) as a MT/MLS or MLT. We are hiring for a permanent and full or part time Hematology Medical Technologist/MLS or MLT on evening/second shift!

New!

Randolph, MAToday

You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min . Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751!

Devens, MA14 days ago

$42.82–$45.42 Per Hour
Full-time
Employee

Position Overview:Client is seeking an engaged, organized, self-driven individual to perform microbiology laboratory testing and evaluate microbial growth characteristics in support of clinical and commercial technology transfers. ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.

Waltham, MA30+ days ago

$221,500–$332,250 Per Year

Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. You will also be assigned to a project and are leading a team of clinical scientists and will be an important part of the project Team, working collaboratively with the program and study level physician or clinical lead as their guide in medical scientific aspects of the compound and its development.

Needham, MA30+ days ago

$133,579–$199,501 Per Year

Author (and/or work with external medical writers to develop) clinical documents including but not limited to clinical protocols/amendments, briefing documents, IND annual reports, Investigators Brochures, clinical study reports, scientific presentations including abstracts, posters and manuscripts. Ensure clinical data collection proceeds in a manner consistent with strategic objectives and regulatory requirements for reporting (i.e., collaborate with statisticians to produce statistical analysis plans and data displays; provide input to CRF design and data management processes; perform periodic review of clinical data).

Cambridge, MA25 days ago

$122,250–$176,583.33 Per Year

Main responsibilities: Contributes to preparation and/or review of any documents related to the studies and requiring a scientific background (abbreviated protocol/protocol/amended protocol, patient written information, presentations/communication to internal or external partners, study reports, committee charters, protocol registration form, redacted protocol, lay summary …). Contributes to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved in study data validation and review processes, support the CRD for the Clinical Case review (safety events reported to GPV or safety events of special interest), notably to anticipate and prevent last minute queries or backlog and smoothen the process.

Cambridge, MA30+ days ago

Remote

Clinical Scientist will ideally be familiar with drug development and regulatory requirements and will deploy this expertise in the execution of a number of key responsibilities: Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support.

New!

Needham, Massachusetts6 days ago

The clinical scientist will provide scientific leadership at the study level, contribute meaningfully to program strategy, and serve as a key partner to cross-functional teams to ensure that clinical development plans, study designs, and data packages are scientifically rigorous, operationally feasible, and aligned with evolving regulatory expectations. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.

Waltham, MA8 days ago

$161,700–$202,200 Per Year

This position works closely with Medical Directors to support medical monitoring activities, while partnering cross-functionally with Clinical Operations, Data Management, Biostatistics, Translational Sciences, Medical Affairs, and Regulatory Affairs to translate clinical strategy into operational deliverables and ensure rigorous ongoing review of trial data for quality, safety, and protocol compliance. Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody.

Boston, MA30+ days ago

Aktis' most-advanced program, AKY-1189, is a miniprotein radioconjugate targeting Nectin-4, with multi-indication potential across multiple tumor types, including locally advanced or metastatic urothelial cancer, breast cancer, non-small cell lung cancer, colorectal cancer, cervical cancer, and head and neck cancer. Deliver quality study strategy and design, including analysis and interpretation of data throughout the study, including leading clinical data review with Data Management; develop and review clinical narratives; and monitor clinical data for specific trends.

New!

Waltham, Massachusetts5 days ago

This role partners closely with Clinical Operations and cross-functional teams to ensure high-quality trial conduct, rigorous data review, and clear scientific communication from study start-up through reporting. Lead ongoing review of clinical trial data listings, including adverse events, laboratory data, concomitant medications, vitals, ECGs, and safety outputs.

Cambridge, MA30+ days ago

Work with some of the brilliant minds of the world solving exciting real-world problems through Artificial Intelligence, Machine Learning, analytics, and insights through triangulating unstructured and structured information from the biomedical literature as well as from large-scale molecular and real-world datasets. Our team brings together computer scientists, biologists, and medical experts (MDs and PhDs) from top universities, creating a fast-paced and innovative environment to solve real-world biomedical challenges.

Watertown, MA30+ days ago

$145,000–$215,000 Per Year

Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Work within a matrix environment, collaborating with medical directors, regulatory affairs, translational medicine, clinical operations, data management, biostatistics, and other departments to drive clinical development programs forward.

Boston, MA30+ days ago

$190,000–$252,000 Per Year

Act as a primary contributor and owner of key clinical deliverables, including: Clinical study protocols and protocol amendments, Investigator's Brochures, Clinical study reports and data summaries, and Regulatory submission documents (e.g., INDs, amendments, briefing materials). As a Clinical Scientist in the Clinical Development group, you will support day-to-day medical monitoring, clinical development, data services, and pharmacovigilance for lead programs, as well as future indications.

Boston, MA30+ days ago

Please be aware of identity thieves actively posing as Takeda employees or recruiters posting Takeda-branded jobs online to steal personal information from job seekers. Clinical Scientist, Neuroimmunology & Specialty Care, PDT at Takeda Pharmaceutical.

Brighton, MA30+ days ago

$170,000–$245,000 Per Year

Position Summary: Aura Biosciences, Inc. is currently expanding its Clinical Development team to support several early- and late-phase clinical assets and is searching for a highly motivated and hands-on Associate Director/Director level Clinical Development Scientist to support the continued development of AU-011 in the treatment of ocular and urologic cancers. Knowledge of and experience applying the principles of clinical research methodology, statistics, data analysis and interpretation Proficiency in data review tools for data interpretation to both design/execute clinical trials and to extract data/prepare results for relevant clinical trials.

Boston, MA30+ days ago

$255,800–$402,700 Per Year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

Cambridge, MA30+ days ago

$154,500–$249,947 Per Year

Level of Education Required: Advanced degree in life science/clinical/medical field, PhD or PharmD Number of Years of Experience in the Function and in the Industry: Minimum of 5+ years of clinical development/research and R&D experience preferred for an Associate Director Level EyePoint is committed to fair and equitable compensation practices. Experience in ophthalmology and familiarity with drug/device combination products Experience with all phases of clinical drug development including regulatory submissions Ability to survey and interpret scientific literature related to the assigned portfolio of products Strong communication, organizational and interpersonal skills are required.

Cambridge Crossing, MA30+ days ago

$159,290–$193,022 Per Year

Proactively provides insight into novel ways to incorporate biomarkers into clinical designs to enable early understanding of emerging drug profiles, as well as input around tumor types and potential impact of biomarkers on internal decision making. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Cambridge, MA28 days ago

$140,300–$189,700 Per Year

Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. Strong knowledge of clinical pharmacology principles in drug development including PKPD, modeling and simulation, ADME concepts, and clinical pharmacology.

Boston, MA30+ days ago

$260,300–$409,700 Per Year

Interface broadly with key functions including Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research throughout research sites around the world. • Contributing to the identification of novel targets by partnering with discovery research teams to bring a clinical perspective into the earliest stages of target identification and validation and executing clinical studies to evaluate the relevance of potential targets to human disease in order to justify investment in clinical development programs.

Waltham, MA25 days ago

In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

Boston, MA30+ days ago

Remote

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Salem, MA12 days ago

Travel Nurse Across America is seeking a qualified Clinical Lab Scientist Lab needed for travel nurse assignment in Salem, MA. This assignment is in a Traveler-friendly facility and offers excellent pay, benefits, bonus opportunity, travel reimbursement, all licenses and certifications paid and more!

New!

Boston, Massachusetts2 days ago

Collaborate with teams across the organization, including clinical operations and data management, to ensure biomarker assay implementation and execution, and aid in the management of biomarker samples and data. The actual salary offered will be based on a number of factors, including but not limited to the qualifications of the applicant, years of relevant experience, level of education attained, certifications or other professional licenses held, and if applicable, the location in which the applicant lives and/or from which they will be performing the job.

Boston, MA30+ days ago

$160,000–$200,000 Per Year

While your primary focus is evaluative, you will be a key player in the broader clinical DS ecosystem, collaborating on patient risk stratification and building the forecasting engines that predict our quality performance across various value-based care programs. Automate Model Lifecycles with AI Agents: Architect and oversee AI-driven agents that autonomously manage the end-to-end lifecycle of our statistical models - leveraging automation for continuous training, deployment, performance monitoring, and proactive model refreshes.

Boston, MA30+ days ago

$122,400–$183,600 Per Year

This role is critical in ensuring the success of clinical manufacturing processes for our cell therapy programs by leading technical investigations, resolving quality events, and driving continuous improvement in analytical development. Cross-Functional Communication and CAPA Implementation: Serve as a liaison between manufacturing, quality control, quality assurance, and analytical development teams to address and resolve quality events.

Framingham, MA30+ days ago

About Variantyx: Variantyx is an award-winning, technology-driven molecular diagnostics lab that offers innovative solutions in the genetic disorders, reproductive health, and precision oncology markets. Responsibilities: Your duties will include interpreting sequence variants in the context of genetic disorders, curating medical and molecular literature, and compiling clinical draft reports.

Waltham, MA30+ days ago

Remote

Collaborate closely with Clinical Operations colleagues on clinical trial activities and timelines, including Informed consent development and review, data management activities and review of data management plans and other documents, and management of clinical development document deliverables to meet the operational needs of the program. Support Clinical Development in the activities associated with execution of clinical trials and data collection, including training of the internal team, vendors, and site staff; preparation of case report forms; identification and prevention of protocol deviations; and resolution of issues.

Cambridge, MA30+ days ago

$176,600–$294,300 Per Year

Provides clinical guidance to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends; reviews and queries data; presents data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical guidance to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and ensures clinical documents are updated in response to emerging safety profile; tracks and reconciles Serious Adverse Events; leads clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.

Cambridge, MA30+ days ago

$214,900–$358,100 Per Year

Boston, MA12 days ago

$193,500–$338,800 Per Year

Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Organization Overview: Verve, a wholly owned subsidiary of Eli Lilly, is seeking a Senior Director - Clinical Research Scientist (CRS) to help lead clinical trial efforts for our innovative gene editing therapies targeting cardiovascular disease.

Cambridge, MA30+ days ago

Qualifications PhD in Chemistry, Biochemistry or related disciplines with 1-4 years industry experience, Master's degree with > 6 years related industry experience or Bachelor's degree with > 10 years related industry experience respectively, with demonstrated chromatographic separation, method development / qualification and structure elucidation expertise. Key Responsibilities Develop, qualify, and troubleshoot chromatographic (GC, HPLC/UPLC) and LCMS based methods for the identification, characterization, and impurity profiling of oligonucleotides, siRNAs, and their formulations, as well as raw material related analytical methods and other methods as needed.

Boston, MA30+ days ago

$113,000–$135,000 Per Year

This role executes on strategic scientific collaborations involving a range of functions and external collaborators, supporting studies that establish the clinical validity and utility of products and biomarkers aligned to Clinical Development Plans and FMI enterprise strategy. Working with Clinical Development leadership, this position will execute analysis for and support studies through conceptualization, narrative building, and writing using clinical cohorts or real-world evidence in partnership with the project lead.

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Clinical Scientist Jobs in Cambridge, MA

Medical Director, Clinical Science - Solid Tumor Takeda Pharmaceutical

Medical Director, Clinical Science, NS TAU- Sleep Medicine Takeda Pharmaceutical

Associate Medical Director, Clinical Science, NS TAU Takeda Pharmaceutical

Research Scientist AI/ML Foundational Models Takeda Pharmaceutical

Medical Laboratory Scientist in Easton, Massachusetts - DAY SHIFT KA Recruiting Inc.

Medical Laboratory Scientist in Southern Massachusetts KA Recruiting Inc.

Medical Laboratory Scientist OR Medical Laboratory Technician on Day Shift KA Recruiting Inc.

Medical Lab Scientist I - Evening Shift Boston Children's Hospital

Per Diem-Medical Lab Scientist Boston Children's Hospital

Medical Lab Scientist I - Overnight Boston Children's Hospital

Medical Lab Scientist I Boston Children's Hospital

Associate Director, Quantitative Clinical Pharmacology (QCP) Lead Takeda Pharmaceutical

Med Tech or MT or Medical Laboratory Scientist or MLS or Medical Laboratory Tech or MLT (Nights) KA Recruiting Inc.

Medical Technologist OR Medical Laboratory Scientist OR MLT in Rhode Island KA Recruiting Inc.

Medical Laboratory Scientist - Massachusetts KA Recruiting Inc.

Med Tech (MT) or Medical Laboratory Scientist (MLS) or Medical Laboratory Tech (MLT) KA Recruiting Inc.

Hematology Medical Laboratory Scientist OR Technician - Full Time or Part Time KA Recruiting Inc.

Part-Time Medical Technologist or Medical Laboratory Scientist in Massachusetts KA Recruiting Inc.

Engineering - Assistant / Associate Scientist Eclaro

Senior Group Director, Clinical Scientist AstraZeneca Plc

Sr. Clinical Scientist/Associate Director, Clinical Science Celldex Therapeutics Inc

Junior Clinical scientist Sanofi

Clinical/Development - Senior Clinical Scientist TalentBurst, Inc.

Clinical Scientist 2, Clinical Development Xenon Pharmaceuticals

Associate Director, Clinical Scientist Zenas BioPharma (USA) LLC

Director, Clinical Scientist Aktis Oncology Inc

Director, Clinical Scientist Kailera Therapeutics

Senior Clinical Scientist nference inc

Senior Manager, Clinical Scientist, Respiratory Kymera Therapeutics Inc

Director, Clinical Scientist Kelonia Therapeutics Inc

Clinical Scientist, Neuroimmunology & Specialty Care, PDT Takeda Pharmaceutical Co Ltd

(Assoc.) Director, Clinical Development Scientist-Urologic Oncology Aura Biosciences Inc

Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co Inc

Associate Director, Clinical Scientist EyePoint Inc

Principal Scientist, Cancer Immunology Clinical Translational Research Bristol-Myers Squibb Co

Sr. Scientist Clinical Pharmacology Alnylam Pharmaceuticals Inc

Clinical Director (Principal Scientist), Translational Medicine, Immunology Merck & Co Inc

Associate Director, Clinical Research Scientist (Neurology) Alkermes Plc

Senior Field Clinical Scientist - Remote Abbott Laboratories

Travel Clinical Lab Scientist (CLS) in Salem, MA TNAA | TotalMed

Sr. Scientist/Principal Scientist, Translational Research and Clinical Biomarkers (Immunology) Antares Therapeutics

Staff Data Scientist, Clinical Performance Latitude Health Inc

Analytical Development Senior Research Scientist, Clinical Manufacturing Investigations Vertex Pharmaceuticals Inc

Clinical Genomic Variant Scientist Variantyx Inc

Clinical Development Scientist Viridian Therapeutics Inc

Director, Clinical Development Scientist (Non-MD) Pfizer Inc

Clinical Development Scientist (Senior Director) Pfizer Inc

Director - Clinical Research Scientist Eli Lilly and Co

Clinical/Development - Scientist TalentBurst, Inc.

Scientist I, Clinical Development Foundation Medicine Inc

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