300 Results for

Clinical Scientist Jobs in Brookline, MA

Jobs

New!

Cambridge, MAToday

$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

$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, MAToday

$198,500–$311,850 Per Year

Boston, MA27 days ago

$40–$48 Per Hour
Contractor

A nationally recognized pediatric academic medical center is seeking an experienced Recruiter to support hiring across clinical research and related scientific roles. This individual will partner closely with hiring managers and research leadership to attract and hire top-tier talent supporting groundbreaking research initiatives.

New!

Westport, 02790, MA1 day ago

The organization partners with healthcare professionals, research teams, and sponsors to deliver high-quality clinical research while maintaining a strong focus on patient safety and regulatory compliance. Candidates who apply for roles through the Atrium website will be added to our candidate pool and may be considered for additional roles of a similar title.

Weymouth, MA8 days ago

In addition, the Research Nurse utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Participates in Division of Nursing / Institute committees at the main DFCI Longwood campus, including, but not limited to, the monthly Research Nurse Practice Committee meeting.

New!

Boston, MA2 days ago

Remote

$55,369.60–$88,576.80

Knowledge and skills necessary to solve complex problems in the areas of clinical/research operations, business planning, financial management, marketing, personnel and information systems management. Supporting the Nursing Science Fellowship (basic overview of fellowship below)To provide a structured program of clinical inquiry scholarship and its use in advancing nursing science.

Boston, MA8 days ago

The successful candidate will play a central role in leading our existing clinical trial infrastructure as well as the design, activation, and conduct of Phase I and first-in-human studies, contribute to the strategic growth of the Phase I program, and provide outstanding clinical care within a collaborative, mission-driven academic medical center. This role is ideal for an early- to mid-career physician-scientist who is prepared to assume increasing leadership in early-phase trial development while continuing to build an independent clinical and translational research portfolio.

New!

Devens, MA6 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.

South Boston, MA30+ days ago

$125,000–$140,000 Per Year

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. Familiarity with ICH, GCP, and relevant regulatory requirements, and strong analytical and strategic thinking skills, experience with interacting with medical monitors, development operations (preclinical, clinical operations, regulatory affairs, Quality Assurance) and clinical investigators.

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, MA30+ days ago

Contribute to interpretation of trial results and draft clinical trial reports - Lead critical assessment of scientific literature including targeted and systematic reviews - Support the team in design and execution of pre-clinical studies - Support regulatory submissions and post-market surveillance activities Wed expect you to be willing to turn your hand to anything within the remit that helps the team deliver its objectives. We offer a competitive salary and a great benefits package including a bonus, non-contributory pension, private healthcare which covers pre-existing conditions, annual personal day for every employee to use however they wish and enhanced global parental leave pay.

Cambridge, MA30+ days ago

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!

Watertown, MAToday

$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. Collaborate 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.

New!

Boston, MA4 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

$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.

Boston, MA30+ days ago

$143,000–$179,000 Per Year

This role executes on strategic scientific collaborations involving a range of functions and external collaborators, driving studies that establish the clinical validity and utility of products and biomarkers aligned to Clinical Development Plans and FMI enterprise strategy. Senior Scientist, Clinical Development is a scientist with translational expertise leading key scientific studies from concept through to publication, focused on the value of FMI's products in clinical practice and oncology drug development.

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.

Cambridge, MA30+ days ago

Full-time

The Scientist, is part of Analytical Development Starting Material Group and will be responsible for Develop, qualify and transfer GC, HPLC, UPLC and mass spectrometry based assays of starting materials, raw materials, intermediates and excipients to suppliers, CMOs and QC. Author and review method development and qualification reports and SOPs for test methods, as well as transfer / qualification protocols and reports related to critical starting materials / intermediates / excipients.

West Roxbury, MA30+ days ago

Operate automated analyzers (Client Architect, Client Alinity, Advanced Instruments Osmos, Polymedco OC80). This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.

New!

Cambridge, MA4 days ago

$144,800–$227,900 Per Year

Required Skills: Alzheimer''s Disease, Biological Research, Biomarker Identification, Biomarkers, Collaborative Research, Computational Biology, Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Detail-Oriented, Genome, Machine Learning (ML), Neurodegenerative Diseases, Neurological Disorders, Neuroscience, Omics, Parkinson''s Disease, Programming Languages, Proteomics, Self Motivation, Stakeholder Relationship Management. They will work alongside other data scientists, geneticists, AI/ML scientists in the department to develop and apply innovative approaches to analyze and integrate proteomics data with WGS, bulk/single-cell/spatial RNAseq, and metabolomics data to identify disease subtypes and predict therapeutic responses of biomarkers and clinical endpoints in specific subgroups of patients.

New!

Cambridge, MAToday

$200,000–$325,000 Per Year

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. New York pay range$200,000—$325,000 USDAt Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves.

Boston, MA30+ days ago

$60,320–$150,009.60 Per Year

Key Responsibilities: • Research and develop deep learning models for MRI reconstruction, segmentation, quantification, and image enhancement • Design, optimize, and evaluate AI pipelines to improve image acquisition efficiency, image quality, and robustness • Integrate AI methods with quantitative CMR imaging biomarkers, including myocardial blood flow, strain, and tissue characterization • Develop and apply methods for multi-modality data integration, combining imaging, physiologic signals (e.g., ECG), genetic, and clinical data for diagnostic and prognostic modeling • Perform rigorous model validation, including reproducibility testing, bias assessment, and external validation • Design, develop, and implement user-friendly software platforms for clinical deployment of AI-enabled imaging tools. USD FLSA: Exempt Req ID: JR89997 330 Brookline Avenue, Boston, MA, 02215 Get directions Get Directions Beth Israel Deaconess Medical Center 330 Brookline Avenue, Boston, MA 02215 Start Mode Car Transit Bike Walk Transit Bus Subway Train Tram Rail Default Fewer transfers Less walking Avoid Tolls Highways Ferries G Google Maps Apple Maps Waze Apple Maps doesn't support Bike mode; we'll open Driving.

New!

Boston, MAToday

Remote

$140,000–$190,000 Per Year

Develop Other Advanced Statistical Models: Create and refine predictive models (Bayesian inference, regression analysis, time-series forecasting) to address other key clinical trial challenges and improve decision-making. Patient Matching/Ranking Algorithms: Support projects to build algorithms that intelligently match patients to (or rank patients for) appropriate clinical trials, enhancing recruitment efficiency and patient inclusion.

New!

Boston, MA2 days ago

$83,200–$312,000 Per Year

For non-bench research, non-clinical staff scientists, knowledge of epidemiology, outcomes research, evidence-based medicine, and experience using longitudinal datasets, data repositories and statistical Analysis with SAS, STATA or SPSS. Problem Solving: Ability to address problems that are broad, complex and abstract, often involving Medical Center-wide issues and requiring substantial creativity, resourcefulness, staff engagement, Lean diagnostic techniques, negotiation and diplomacy to develop solutions.

Boston30+ days ago

$170,000–$215,000 Per Year

ResponsibilitiesLead and execute complex data science projects that directly advance our drug development portfolioDevelop and implement sophisticated models for therapeutic hypothesis evaluation including patient stratification and biomarker identificationDesign and create AI models for modernizing clinical trial evaluations including surrogate endpointsAid in the development and training of AI agents to automate and optimize biomedical workflowsCollaborate cross-functionally with clinical technical and research teamsPresent complex analytical findings to senior stakeholders including executive leadershipAbout YouRequired QualificationsPhD in computational sciences or life sciences3 years of post-academic experience in life sciences biotech pharma consultingStrong programming skills particularly in PythonExtensive experience in multi-modal bioinformatics analysisPreferred QualificationsProven expertise in cloud computing environments including proficiency with tabular andor graph databasesStrong background in machine learning and deep learning particularly in biological applicationsExperience with large language models LLMDemonstrated ability to collaborate effectively with engineering teams on production systemsStrong communication skills with proven ability to present complex technical findings to senior stakeholdersCompensationSalary ranges are informed in part by geographic location in addition to other factors. Formation Bio partners acquires or in-licenses drugs from pharma companies research organizations and biotechs to develop programs past clinical proof of concept and beyond ultimately helping to bring new medicines to patients.

New!

Westborough, MA3 days ago

Deep expertise in designing and executing global clinical evidence generation programs, including protocol development, study design, endpoint strategy, clinical study report development, and integrated publication planning to support regulatory, reimbursement, scientific, and commercial objectives. In addition to leading evidence generation strategies for product development, regulatory approval, and reimbursement, this role serves as a clinical thought leader, translating complex global insights into actionable strategies that accelerate commercialization and adoption.

New!

Boston, MA4 days ago

$104,000–$112,320 Per Year

Eurofins Scientific is a global leader in life sciences, delivering a broad range of analytical testing services across industries including pharmaceuticals, food, environmental, and clinical research. We are seeking a Scientist - Off-Target Genomics (Gene Therapy) to lead and execute genomic safety assessment strategies for gene editing therapeutics.

New!

Cambridge, MA3 days ago

$93,800–$174,200 Per Year

Key Responsibilities, include, but are not limited to:Design, develop, troubleshoot, and optimize immunological assays-such as flow cytometry and single-cell profiling-and implement advanced technologies like single-cell RNA sequencing and multiplexed imaging to characterize immune cell populations and identify biomarkers from peripheral blood and tissues. Senior Scientist I: Bachelor's degree in cell and molecular biology or a related discipline with at least 5 years of relevant work experience; or Master's degree in cancer immunology or a related discipline with a minimum of 3 years of relevant work experience.

New!

Devens, MA6 days ago

$40–$42 Per Hour

SummaryManufacturing Science & Technology (MS&T), Aseptic & Microbial Process Control Sciences (AMPCS), 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. Key responsibilities and projects:Support Clinical and Commercial Tech Transfers Project: Perform Microbial Characteristics Testing.

Cambridge, MA30+ days ago

$138,600–$257,400 Per Year

The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs.

New!

Boston, MA4 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 his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area.

New!

Cambridge, MA3 days ago

$148,000–$203,500 Per Year

Flagship has been recognized twice on FORTUNE's "Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been named four times to Fast Company's annual list of the World's Most Innovative Companies. Harnessing the drug development expertise of its team together with the power of Flagship''s multiple scientific platforms, Pioneering Medicines explores and identifies new product concepts which are then advanced jointly with Flagship's bioplatform companies.

New!

Cambridge Crossing, MA4 days ago

$137,570–$166,706 Per Year

Proficient with molecular and cellular biology related techniques, including but not limited to 2D/3D/spheroid cell culture and related cellular assays, Western blot and/or JESS, qRT-PCR, flow cytometry, proliferation and/or cytotoxicity assays (CyQuant, CTG, apoptosis, IncuCyte, etc.), ELISA, MSD and/or HTRF assays, colony formation assay, processing of DNA/RNA/protein, IP/Co-IP. In addition, the individual will coordinate with other functions, such as informatics and predictive science, lead discovery and optimization, in vivo pharmacology, and translational research teams to design/execute work related to patient stratification, identification of appropriate PD markers and assay development/transfer for miniaturization, among others to ensure timely project advancement.

Boston, MA30+ days ago

We are seeking a Statistical Geneticist with expertise in whole genome sequencing (WGS), proteomics, and clinical outcomes analysis to advance our research in identifying novel therapeutic targets. The Cardiometabolic Research (CMR) Therapeutic Area of our client, focuses on the discovery of biologic, small molecule and genetic therapeutics for the treatment of cardiometabolic diseases and associated complications.

Cambridge, MA30+ days ago

Responsibilities: Complete routine PD-grade viral vector production operations at both bench scale and pilot scale, including but not limited to media preparation, culture initiation, seed train maintenance and bioreactor operations, to support process development studies and material generation for pre-clinical programs. Associate Scientist is responsible for the development of robust, efficient, scalable and transferable lentiviral vector (LVV) manufacturing for early and late-stage cell therapy programs, for both ex-vivo and in-vivo delivery approaches.

New!

Cambridge, MA4 days ago

$89,925–$149,875 Per Year

Preferred Qualifications: If you have the following characteristics, it would be a plus: PhD with experience in viral immunology or infectious disease Experience with in vivo viral challenge models Experience working with multiple species Strong experience with immune-response related readout methods such as ELISA, Flow, Luminex, or qPCR methodologies. You will help design and write in vivo study protocols, coordinate and initiate preclinical studies, conduct experiments and analyze experimental data pertaining to the understanding of cellular mediated immune responses and humoral immune responses from novel vaccine candidates, formulations, and platforms.

Boston, MA30+ days ago

$154,500–$202,000 Per Year

The skills you develop here - portfolio construction over assets with radically asymmetric risk profiles, clinical trial analytics, AI/ML in production, and risk management across multi-year horizons - can directly impact the delivery of new and effective therapeutics to patients by best aligning impactful medicines with economic incentives. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials.

New!

Boston, MA5 days ago

$210,400–$331,100 Per Year

The Distinguished Scientist/ Executive Director within Companion Diagnostics (CDx) Development, will lead one of our company's Diagnostic Development Teams (DxDTs), supervising PhD-/MD-level employees, developing and overseeing CDx strategy development, alignment and execution for specific projects, including associated digital pathology (DP) projects when applicable. Primary Responsibilities: Lead cross-functional DxDT including Regulatory, Commercial, Business Development, Project Management, Operations, Clinical Development, Statistics, Bioinformatics, etc. to drive CDx strategy, development and implementation of CDx projects - and associated DP when relevant - for a portfolio of various assets/biomarkers, mainly in the therapeutic area of Oncology.

New!

Boston, MAToday

PhaseV (HQ in Boston, R&D in Tel Aviv) is a cutting-edge startup, pushing innovation in the drug development process to bring new treatments to more patients, in a more efficient and precise way. Collaborating with 7 of the top pharmaceutical companies, as well as multiple CROs and biotechs, we are poised to make a significant impact on how drugs are developed and brought to market.

New!

Cambridge, MA5 days ago

$139,840–$209,760 Per Year

The primary responsibilities of the Principal Scientist are to: Responsible for identifying and setting up relevant mechanistic and disease in vivo models to support cardiovascular and renal projects from target identification to preclinical candidate acceptance and early clinical development including hands-on experimentation, analysis of data and presentation to cross-functional project teams; Prepare and update experimental protocols; Independently perform data analysis and effectively interpret results; Support evaluation of external innovation landscape in the field of in vivo models and connection to external partners (CROs, academic partners); Lead novel target proposals and experimental validation to support growth of our early cardiovascular & renal portfolio including presentation at internal governance; Support BD&L assessment of external targets and programs to understand the competitive landscape and identify potential opportunities for collaboration or technological innovation; Engage in close collaboration with scientists and technical staff of the In Vivo Cluster based at the German sites to share knowledge, drive progress and stimulate innovation; Lead publication of results, prepare reports and presentations at both internal and external forums; Coach research associates in a matrix organization; Collaborate effectively with colleagues and interdisciplinary teams both within Bayer and with external collaborators; Ensure that all tasks are aligned with respect to HSE guidelines, animal welfare law and regulations, documentation guidelines, and good research practices. Specifically, the candidate will design and conduct experimental research studies at the bench, coach research associates, and propose therapeutics project(s) targeting cardiac or renal (including cardio-renal metabolic) disease.

Cambridge, MA23 days ago

Full-time

The DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. Experience with structural modeling tools and frameworks, including protein structure prediction (AlphaFold2/3, RoseTTAFold, ESMFold), structure-based design (ProteinMPNN, RFdiffusion), and/or graph neural networks operating on 3D protein coordinates (e.g.

Manchester, NH23 days ago

The Advanced Regenerative Manufacturing Institute (ARMl)IBioFabUSA is a Member-based non-profit, member-driven, public-private partnership with a mission to advance the bioeconomy and transform the future of human health. The ideal candidate will have experience with process development or early phase GMP manufacturing, aseptic techniques and operations within a controlled manufacturing environment, SOP/Batch Record drafting, and other aspects of contract manufacturing.

New!

Cambridge, MA3 days ago

$114,100–$211,900 Per Year

Principal Scientist I: 3+ year of postdoctoral trainingPrincipal Scientist II: Completed post-doctoral training plus 3+ years of industry experiencePhD in oncology, immunology, cell biology, biochemistry, molecular biology or a related disciplineStrong scientific acumen and in-depth mechanistic understanding of cancer biology and the tumor immune microenvironment. We are seeking a highly motivated and innovative Principal Scientist (I or II) to provide translational leadership in support of Novartis' oncology portfolio, including cell and gene therapies (e.g., CAR-T), biologics, antibody-drug conjugates, immune cell engagers, and targeted therapies.

Boston, MA18 days ago

Key ResponsibilitiesProducing innovative solutions driven by exploratory data analysis of complex and high-dimensional datasets; applying knowledge of statistics, machine learning, programming, data modeling, and advanced mathematics to generate and test hypotheses and interpret the results of experiments. Presenting at project and internal meetings; effectively conveying progress and asserting point of view; constructively discussing issues and providing facts; building credibility and trust by asking thoughtful questions and actively listening; running productive project meetings that advance problem-solving.

Boston, MA30+ days ago

Professional coding expertise in languages like Python and Go, proficiency in SQL, and experience with data visualization tools; skilled in using ML frameworks (TensorFlow, PyTorch) and implementing CI/CD, containerization, and version control best practices. Professional coding expertise in languages like Python and R, proficiency in SQL, and experience with data visualization tools; skilled in using ML frameworks (TensorFlow, PyTorch) and implementing CI/CD, containerization, and version control best practices.

West Roxbury, Massachusetts30+ days ago

$40–$45 Per Hour

The employee will perform routine chemistry and urinalysis testing using automated instrumentation, including Beckman Coulter Urinalysis systems, Advanced Instruments Osmos, Polymedco OC80, and manual urinalysis and chemistry methods. The employee will perform routine chemistry testing using automated instrumentation, including Abbott Architect ci8200, Abbott Alinity, Advanced Instruments Osmos, Polymedco OC80, and manual chemistry methods.

Watertown, MA30+ days ago

$145,000–$215,000 Per Year

Partner closely with CMC colleagues and QA to (i) write or review test methods, SOPs, analytical data summaries (CoT/CoA), protocols, and technical reports, (ii) critically review, trend, and interpret analytical testing results, and (iii) support investigation of nonconformances (OOS/OOT results, deviations, etc.). 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.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Clinical Scientist job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Clinical Scientist Jobs in Brookline, MA

Associate Medical Director, Clinical Science, NS TAU- Neurology/Psychiatry Takeda Pharmaceutical

Medical Director, Clinical Science - Solid Tumor Takeda Pharmaceutical

Associate Medical Director, Clinical Science, NS TAU Takeda Pharmaceutical

Healthcare Recruiter (Clinical & Research Talent) Workforce Connections

Clinical Research Medical Director (Part-Time) Atrium

RN Clinical Research Nurse / Dana-Farber Cancer Center South Shore Health

Senior Program Coordinator Boston Children's Hospital

Medical Oncologist - Multiple Disease Site Options Tufts Medicine

Engineering - Assistant / Associate Scientist Eclaro

Clinical Scientist/ Senior Clinical Scientist CRISPR Therapeutics AG

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

(Senior) Clinical Scientist CMR Surgical Ltd

Clinical/Development - Senior Clinical Scientist TalentBurst, Inc.

Senior Manager, Clinical Scientist, Respiratory Kymera Therapeutics

Director - Clinical Research Scientist Eli Lilly and Co

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

Sr Scientist, Clinical Development Foundation Medicine Inc

Clinical/Development - Scientist TalentBurst, Inc.

Clinical/Development - Scientist, Analytical Development LanceSoft Inc

Medical Technologist (Clinical Laboratory Scientist MT/MLS/CLS) LanceSoft Inc

Senior Data Scientist, Neuroscience Biomarker Discovery Merck & Co Inc

Staff Data Scientist Iterative Health

Staff Scientist I - Quantitative MRI & Generative AI for Cardiovascular Imaging Lahey Hospital and Medical Center

Senior Data Scientist OneStudyTeam

Staff Scientist II - PhD Biostatistician Lahey Hospital and Medical Center

Senior Data Scientist Formation Bio Inc

Director, Clinical Research GI ET Olympus Corp

Scientist - Off-Target Genomics (Gene Therapy) Eurofins Scientific SE

Senior Scientist I / II - Translational Immuno‑Oncology Research (OTR) Novartis AG

Assistant/Associate Scientist Sunrise Systems Inc

Senior Principal Scientist/Associate Director PK Sciences (DUAL LEVEL POSTING) Novartis AG

Clinical Director, Clinical Research, Ophthalmology Merck & Co Inc

Pioneering Medicines: Principal Scientist / Senior Principal Scientist, Bioanalytical Lead | Drug Metabolism & Pharmacokinetics Flagship Pioneering Inc

Senior Scientist, Discovery Biology Oncology Bristol-Myers Squibb Co

Post Doctoral Scientist- Human Genomics and Translational Data Science Xenon7

Associate Scientist Karwell Technologies

Scientist, In Vivo Immunology GSK plc

Data Scientist - Portfolio Optimization Formation Bio Inc

Distinguished Scientist, Companion Diagnostics Merck & Co Inc

Senior Data Scientist PhaseV

Principal Scientist - In Vivo Expert, CVRI (Cardiovascular, Renal & Immunology) Bayer AG

Applied Machine Learning/AI Scientist Repertoire Immune Medicines

Scientist Advanced Regenerative Manufacturing Institute Inc

Principal Scientist I / II - Translational Immuno‑Oncology Research (OTR) Novartis AG

Genomic Scientist Boston Children's Hospital

Machine Learning Scientist II - Multimodal AI Wayfair

Medical Laboratory Scientist Aptive

Principal Scientist, Analytical Development Kymera Therapeutics

Resume Resources