JouléNewGlobal Pathology Quality Control Scientist JouléGlobal Pathology Quality Control Scientist06340, CT$50–$56.70 / hourSystem One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. Conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens, and reports on GLP and non-GLP studies.
Genesis10Histology Scientist Genesis10Histology ScientistRidgefield, CTTemporaryContractorFull timeThe ideal candidate will execute tissue processing, embedding, and staining procedures, including immunohistochemistry (IHC) and immunofluorescence (IF), while collaborating with researchers to design experiments and interpret findings. PhD or Master’s degree in biology, biomedical sciences, or a related field (bachelor’s degree with significant relevant experience may be considered).
Spectraforce Technologies IncScientist II Spectraforce Technologies IncScientist IIRidgefield, CT$61,500–$96,590 / yearEducation : Bachelor’s Degree from an accredited institution with three-plus (3+) years of experience in related scientific discipline or Master’s Degree from an accredited institution in related scientific discipline or equivalent experience in related field. Experience with technologies and instrumentation such as Quant Studio 12K Flex, MSD, Protein WES, Qubit, Nanodrop, 10X Genomics, BioMek i7, Agilent Tapestation and Illumina sequencing platforms is highly preferred.
Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical Science Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical ScienceNew Haven, CT$133,579–$199,501 / yearAuthor (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).
AstraZeneca PlcDevelopment Scientist III, Analytical Development and Clinical Quality Control AstraZeneca PlcDevelopment Scientist III, Analytical Development and Clinical Quality ControlNew Haven, CT$138,392–$207,590 / yearIntroduction to role: The Development Scientist III position is a technical position responsible for development, qualification, and optimization of bioassay (biological activity/potency assay of drug candidates) and process-derived impurity methods (HCP, residual Protein A, residual DNA), in order to support release and stability testing of biotherapeutic products, and also formulation and process development. D. or master's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Chemistry, Bioengineering or related discipline with a minimum of 6+ years of analytical method development and qualification experience in pharmaceutical or biotechnology setting, with high preference in ELISA binding assay, enzymatic assay, cell-based assay, and process-derived impurity methods.
Alexion Pharmaceuticals IncScientist III, Analytical Development and Clinical QC Alexion Pharmaceuticals IncScientist III, Analytical Development and Clinical QCNew Haven, CTStrong command of ICH (Q5E, Q6B, Q8-Q12), USP/EP, FDA/EMA expectations for biologics, GMP/GLP compliance, and authoring/reviewing CTD Module 3, IND/IMPD, BLA/MAA analytical sections and responses to agency queries. Technical expertise in chromatography (e.g., SEC, RP, IEX), capillary electrophoresis (CE-SDS, cIEF), spectroscopy (UV/Vis, fluorescence, CD), bioassays (binding, potency), and residuals/impurities testing (HCP, DNA, residual Protein A).
Boehringer Ingelheim International GmbHSenior Scientist, Non Clinical Drug Safety Boehringer Ingelheim International GmbHSenior Scientist, Non Clinical Drug SafetyRidgefield, CT$140,000–$222,000 / yearIndependently performs scientific experiments with a predefined goal including developing new methodologies, protocols and or test procedures that contribute to core group/research goals and reflect expert knowledge; May direct and oversee experimental design and results of technicians and junior level scientists. Develops expertise in a specific project-relevant area or technology; May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects; Ability to work with various LIMS; Compilation of associated outputs with supervision.
Pfizer IncClinical Development Scientist (Senior Director) Pfizer IncClinical Development Scientist (Senior Director)Groton, CT$214,900–$358,100 / yearProvides 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.
Pfizer IncDirector, Clinical Development Scientist (Non-MD) Pfizer IncDirector, Clinical Development Scientist (Non-MD)Groton, CT$176,600–$294,300 / yearProvides 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.
Boehringer Ingelheim(Senior) Associate Director, Principal Clinical Data Scientist -Early Oncology ExpMed(Remote) Boehringer Ingelheim(Senior) Associate Director, Principal Clinical Data Scientist -Early Oncology ExpMed(Remote)Ridgefield, CTRemote$140,000–$222,000 / yearSupport the early Oncology clinical drug research and development process by providing strategic planning and execution, including clinical trial design and all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data related to clinical projects like actual trial data, registries and real-world data bases. In addition to what is listed above, you will also be responsible for the following: + Subject Matter Expert (SME) / Process Lead for designing, transforming, analyzing and reporting complex early Oncology clinical trials or projects, that represent new challenges and for which project and therapeutic knowledge is not given.
Alexion Pharmaceuticals IncDevelopment Scientist III, Analytical Development and Clinical Quality Control Alexion Pharmaceuticals IncDevelopment Scientist III, Analytical Development and Clinical Quality ControlNew Haven, CT$138,392–$207,590 / yearIntroduction to role: The Development Scientist III position is a technical position responsible for development, qualification, and optimization of bioassay (biological activity/potency assay of drug candidates) and process-derived impurity methods (HCP, residual Protein A, residual DNA), in order to support release and stability testing of biotherapeutic products, and also formulation and process development. D. or master's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Chemistry, Bioengineering or related discipline with a minimum of 6+ years of analytical method development and qualification experience in pharmaceutical or biotechnology setting, with high preference in ELISA binding assay, enzymatic assay, cell-based assay, and process-derived impurity methods.
Summit Health IncClinical Lab Scientist Summit Health IncClinical Lab ScientistNew Britain, CTWe are innovating value-based care and leveraging integrated applications, population insights and staffing expertise to ensure all patients have access to high-quality, connected care services that provide better outcomes at a reduced total cost of care. Our primary, multispecialty, and urgent care providers serve millions of patients in traditional practices, patients' homes and virtually through VillageMD and our operating companies Village Medical, Village Medical at Home, Summit Health, CityMD, and Starling Physicians.
Pfizer IncOncology Clinical Development Scientist, Director Pfizer IncOncology Clinical Development Scientist, DirectorGroton, CT$176,600–$294,300 / yearFollow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate.
Pfizer IncOncology Clinical Development Scientists (Senior Manager) Pfizer IncOncology Clinical Development Scientists (Senior Manager)Groton, CT$139,100–$231,900 / yearFollow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate.
Pfizer IncOncology Clinical Development Scientist (Director) Pfizer IncOncology Clinical Development Scientist (Director)Groton, CT$176,600–$294,300 / yearFollow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate.
Alexion Pharmaceuticals IncDevelopment Scientist II, Analytical Development and Clinical QC (ADQC) Alexion Pharmaceuticals IncDevelopment Scientist II, Analytical Development and Clinical QC (ADQC)New Haven, CTYou will be responsible for: Responsible for generating and/or mirroring, reviewing, providing assessments, and driving ownership of LIRs to close out Out-of-Specification (OOS), Out-of-Trend (OOT), and atypical results with structured root cause analysis, impact assessment, and/or corrective/preventive actions (CAPAs). This candidate will be responsible for initiation and ownership of laboratory investigations (LIRs) through strong liaison with external contract laboratories and change controls relevant to ADQC biologic programs.
The Fountain Group LLCUSA - Bench Scientist - III - USD The Fountain Group LLCUSA - Bench Scientist - III - USDGroton, CTJob Description:The Global Pathology Quality Control Scientist leverages expertise in anatomic and/or clinical pathology techniques and processes to independently perform all aspects of quality control for pathology data, specimens, and reports associated with GLP and non-GLP studies. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners.
MindlanceUSA - Bench Scientist - III - USD MindlanceUSA - Bench Scientist - III - USDGroton, CT$50–$51.40 / hourThrough their expert knowledge in anatomic and/or clinical pathology techniques and processes, the Global Pathology Quality Control Scientist will primarily and independently conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens and reports on GLP and non GLP studies. • Interacts with others in the Pathology line, including anatomic and/or clinical Pathologists, Anatomic and Investigative Laboratory Managers, Anatomic and Investigative Pathology Scientists and Technicians, Clinical Pathology Scientists, Global pathology Slide Scanning Lead .
Integrated Resources, IncBench Scientist - III Integrated Resources, IncBench Scientist - IIIGroton, CTThe Global Pathology Quality Control Scientist independently performs quality control (QC) reviews of anatomic and/or clinical pathology data, specimens, and reports for GLP and non-GLP studies. This role supports candidate selection, first-in-human studies, early research, Client safety, and investigative pathology work through accurate and compliant pathology data review.
Artech LLCScientist|ALX|US Artech LLCScientist|ALX|USNew Haven, CT$60–$64.28 / hourThe primary responsibilities include: (1) lead an inter-department project or initiative involving other contributors; (2) design and execution of innovative scientific experiments for development, validation, and implementation of robust bioanalytical methods on various technology platforms in clinical and nonclinical study samples; (3) develop and implement new and novel protocols to address specific issues and/or troubleshoot and improve current existing assay platforms towards being more robust and transferable. • Serve as part of the BA sub-team, working with Bioanalytical project lead to support discovery or development projects for method qualification/validation, data reporting, and interpretation of issues associated with the bioanalytical results.
Aequor Technologies LLCBench Scientist - III Aequor Technologies LLCBench Scientist - IIIGroton, CTThrough their expert knowledge in anatomic and/or clinical pathology techniques and processes, the Global Pathology Quality Control Scientist will primarily and independently conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens and reports on GLP and non GLP studies. " Interacts with others in the Pathology line, including anatomic and/or clinical Pathologists, Anatomic and Investigative Laboratory Managers, Anatomic and Investigative Pathology Scientists and Technicians, Clinical Pathology Scientists, Global pathology Slide Scanning Lead .
Deloitte Touche Tohmatsu LtdSenior Data Scientist - SFL Scientific Deloitte Touche Tohmatsu LtdSenior Data Scientist - SFL ScientificStamford, CT$128,000–$252,500 / yearWorking with a team of interdisciplinary data scientists, engineers, architects, and consultants, our work includes novel areas such as cancer detection, drug discovery, optimizing population health and clinical trials, autonomous systems and edge AI, agentic solutions, and consumer product innovation. From strategy to execution, this team delivers integrated, end-to-end support and advisory services covering valuation modeling, cost optimization, restructuring, business design and transformation, infrastructure and real estate, mergers and acquisitions (M&A), and sustainability.
Deloitte Touche Tohmatsu LtdData Scientist Engineer - SFL Scientific Deloitte Touche Tohmatsu LtdData Scientist Engineer - SFL ScientificStamford, CT$95,600–$188,400 / yearWorking with a team of interdisciplinary data scientists, engineers, architects, and consultants, our work includes novel areas such as cancer detection, drug discovery, optimizing population health and clinical trials, autonomous systems and edge AI, agentic solutions and framework design, and consumer product innovation. From strategy to execution, this team delivers integrated, end-to-end support and advisory services covering valuation modeling, cost optimization, restructuring, business design and transformation, infrastructure and real estate, mergers and acquisitions (M&A), and sustainability.
LancesoftBench Scientist - III LancesoftBench Scientist - IIIGroton, CT$45Through their expert knowledge in anatomic and/or clinical pathology techniques and processes, the Global Pathology Quality Control Scientist will primarily and independently conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens and reports on GLP and non GLP studies. Interacts with others in the Pathology line, including anatomic and/or clinical Pathologists, Anatomic and Investigative Laboratory Managers, Anatomic and Investigative Pathology Scientists and Technicians, Clinical Pathology Scientists, Global pathology Slide Scanning Lead .
Quest Diagnostics IncMedical Laboratory Scientist I Quest Diagnostics IncMedical Laboratory Scientist IWallingford Center, CT$32.63–$35.79 / hourQualifications: Education: BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. Pay range: $32.63 - $35.79 / hour; employee may be eligible to receive shift differential of 10% for some or all hours worked on second shift and 15% for some or all hours worked on third shift.
CEDENTSenior Scientist CEDENTSenior ScientistBranford, CTWe're hiring a Senior or Principal Scientist to join our Biotherapeutics team's collaborative group focused on designing and advancing first-in-class immune-engaging biologics. Why You’ll Love Working HereDirect impact: Your ideas and experiments will influence platform design and help shape clinical programs.
LancesoftScientist LancesoftScientistGuilford, CT$35Bachelor’s degree in molecular biology or similar field with 2+ years of industry/academic experience, Master’s degree with limited experience, or equivalent work experience. In this role, you will be part of a diverse technology team, ensuring accurate operation of sample preparation, instrument calibration and operation, and data analysis.
Hartford HealthCare CorpSr Scientist Project Manager - Research Design And Support Hartford HealthCare CorpSr Scientist Project Manager - Research Design And SupportHartford, CTJob Summary: The Research Administration Senior Scientist position supports Hartford HealthCare (HHC) research investigators in the design, analysis and review of all research projects, including preparation of abstracts, posters, and manuscripts. Doctoral degree with minimum 3 to 5 years research experience, including complex biostatistical analyses of clinical data, work with databases, and grant writing.
Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Per Diem Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Per DiemBridgeport, CTBachelor''s degree from a regionally accredited college/university with 16 semester hours (24 quarter hours) in biology including one semester in microbiology and 16 semester hours (24 quarter hours) in chemistry including one semester in organic or biochemistry, which may be obtained within, or in addition to, the Bachelor''s degree. It includes a 473-bed community teaching hospital, a 76-bed inpatient psychiatric facility in Westport, a large multispecialty provider group, and special needs services for adults and children.
Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Lab Transfusion Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Lab TransfusionHartford, CTBachelor''s degree from a regionally accredited college/university with 16 semester hours (24 quarter hours) in biology including one semester in microbiology and 16 semester hours (24 quarter hours) in chemistry including one semester in organic or biochemistry, which may be obtained within, or in addition to, the Bachelor''s degree. Job Description: The Medical Laboratory Scientist (MLS) performs, interprets and correlates clinical laboratory tests by following protocols to assist in the physician diagnosis and treatment of illness and disease.
Hartford HealthCare CorpMedical Lab Scientist II - Lab Microbiology Hartford HealthCare CorpMedical Lab Scientist II - Lab MicrobiologyManchester, CTIt includes Manchester Memorial Hospital, a 249-bed community hospital, Rockville General, a campus of Manchester Memorial Hospital, a 102-bed facility, a large multispecialty provider group and visiting nurse services. POSITION SUMMARY: Performs applied techniques for various chemical, microscopic, immunologic and/or microbiological tests to obtain data for use in the diagnosis and treatment of disease.
Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Lab Microbiology Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) - Lab MicrobiologyHartford, CTBachelor''s degree from a regionally accredited college/university with 16 semester hours (24 quarter hours) in biology including one semester in microbiology and 16 semester hours (24 quarter hours) in chemistry including one semester in organic or biochemistry, which may be obtained within, or in addition to, the Bachelor''s degree. This is made possible by being home to the largest robotic surgery center in the Northeast and the Center for Education, Simulation and Innovation (CESI), one of the most-advanced medical simulation training centers in the world.
AlexionAssociate Scientist II, Process Analytical Sciences AlexionAssociate Scientist II, Process Analytical SciencesNew Haven, ConnecticutPerforming routine support testing and optimization of phase-appropriate analytical test methods including capillary electrophoresis (cIEF and CE-SDS), ELISA, various HPLC and UPLC methods (SEC, AEX, glycan analysis) and spectrophotometric applications for evaluation of therapeutic proteins. The Associate Scientist II will be responsible for performing assigned experimental tasks to support development and optimization of manufacturing processes or analytical/characterization methods in addition to clinical stability and release testing for Alexion’s biotherapeutic candidates.
Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS) Hartford HealthCare CorpMedical Laboratory Scientist (MLT, MLS)Avon, CTBachelor''s degree from a regionally accredited college/university with 16 semester hours (24 quarter hours) in biology including one semester in microbiology and 16 semester hours (24 quarter hours) in chemistry including one semester in organic or biochemistry, which may be obtained within, or in addition to, the Bachelor''s degree. The Medical Laboratory Scientist (MLT, MLS) Performs, interprets and correlates clinical laboratory tests by following protocols to assist in the physician diagnosis and treatment of illness and disease.
Penfield Search PartnersPrincipal Real World Evidence (RWE) Scientist Penfield Search PartnersPrincipal Real World Evidence (RWE) ScientistFairfield, CTContact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.comNo 3rd party candidatesBrief Description: The Principal Real World Evidence (RWE) Scientist (Contractor) will provide scientific and analytical leadership for real world evidence generation using large healthcare data sources, including administrative claims and electronic medical records (EMR). Support the design and execution of RWE studies or internal analytic projects using administrative claims and EMR data, including development of research protocols and input into statistical analysis plans (SAPs).
Integrated Resources, IncScientist II Bioanalytical Development Integrated Resources, IncScientist II Bioanalytical DevelopmentNew Haven, CTThe primary responsibilities include: (1) Lead an inter-department project or initiative involving other contributors; (2) Design and execution of innovative scientific experiments for development, validation and implementation of robust bioanalytical methods on various technology platforms in clinical and nonclinical study samples; (3) Develop and implement new and Client protocols to address specific issues and/or troubleshoot and improve current existing assay platforms towards being more robust and transferable. Serve as part of the BA sub-team, working with Bioanalytical project lead to support discovery or development projects for method qualification/validation, data reporting, and interpretation of issues associated with the bioanalytical results.
Eurofins Scientific SEAssociate Materials Scientist Eurofins Scientific SEAssociate Materials ScientistGroton, CTThe Associate Scientist provides laboratory support in synthesizing salt forms of drug candidates and polymorphs, evaluates these forms for acceptability as drug substance as it relates to chemical manufacturing and formulation into pharmaceutical products, and is responsible for writing sections of reports for regulatory submissions. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
PerkinElmerCell Services Scientist PerkinElmerCell Services ScientistNew Haven, ConnecticutThe person needs to occasionally move between labs, corridors, adjoining rooms, and buildings onsite Frequently operate on instruments, objects, tools or controls, which will require regularly bending, squatting, stretching and reaching in order to perform in a service function. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.
Eurofins Scientific SESolid‑State Chemistry Scientist Eurofins Scientific SESolid‑State Chemistry ScientistGroton, CTIt is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins Scientific SENewSenior Materials Scientist Eurofins Scientific SESenior Materials ScientistGroton, CTIt is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Boehringer Ingelheim International GmbHSenior Scientist, Drug Metabolism and Pharmacokinetics - Bioanalysis Boehringer Ingelheim International GmbHSenior Scientist, Drug Metabolism and Pharmacokinetics - BioanalysisRidgefield, CT$140,000–$222,000 / yearThe main responsibilities of the Senior Scientist include: independently developing, troubleshooting, and validating GLP/GCP bioanalytical immunoassay methods with minimal or no supervision, investigation and implementation of new technologies, training/mentoring of junior scientists, monitoring of outsourced bioanalytical work, and may include DMPK representation on project teams. Develops expertise in a specific project-relevant area or technology; May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects; Ability to work with various LIMS; Compilation of associated outputs with supervision.
Bio-TechneProduct Support Scientist Bio-TechneProduct Support ScientistWallingford, ConnecticutWe are seeking a proactive and solutions‑driven Product Support Scientist to advance the performance, reliability, and customer success of our automated microfluidic‑based biomarker analysis platform. This is an exciting opportunity to make a meaningful impact within a fast‑paced, customer‑focused organization dedicated to delivering high‑quality solutions to the fluid biomarker research community.
PerkinElmer US LLCCell Services Scientist PerkinElmer US LLCCell Services ScientistNew Haven, CT$60,000–$80,000 / yearThe person needs to occasionally move between labs, corridors, adjoining rooms, and buildings onsite Frequently operate on instruments, objects, tools or controls, which will require regularly bending, squatting, stretching and reaching in order to perform in a service function. Basic Qualifications: Master of Science in cell biology or related discipline plus 1-2 years of related work experience OR a Bachelor of Science in cell biology or related discipline plus 3-4 years of related work experience.
Alexion Pharmaceuticals IncAssociate Scientist II, Process Analytical Sciences Alexion Pharmaceuticals IncAssociate Scientist II, Process Analytical SciencesNew Haven, CTYou will be responsible for: Performing routine support testing and optimization of phase-appropriate analytical test methods including capillary electrophoresis (cIEF and CE-SDS), ELISA, various HPLC and UPLC methods (SEC, AEX, glycan analysis) and spectrophotometric applications for evaluation of therapeutic proteins. This is what you will do: The Associate Scientist II will be responsible for performing assigned experimental tasks to support development and optimization of manufacturing processes or analytical/characterization methods in addition to clinical stability and release testing for Alexion's biotherapeutic candidates.
Arvinas IncDMPK Scientist Arvinas IncDMPK ScientistNew Haven, CTArvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-102, targeting LRRK2 for neurodegenerative diseases; ARV-806, targeting KRAS G12D for mutated cancers, including pancreatic, colorectal, and non-small cell lung cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle; and vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer. The incumbent will contribute as a DMPK scientist on project teams from drug discovery through all stages of drug development, with a scientific background on key aspects of DMPK science, including but not limited to in vitro and in vivo ADME, animal PK, toxicokinetics, drug metabolism, DME- and transporter-based DDI, 14C-ADME studies, QWBA, human PK prediction.
PfizerSenior Principal Scientist PfizerSenior Principal ScientistGroton, CT$120,800–$201,400 / yearCandidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Pfizer IncSenior Scientist, Process Development Pfizer IncSenior Scientist, Process DevelopmentGroton, CT$93,600–$156,000 / yearThe successful candidate will collaborate closely with chemists, analysts, biochemists, and chemical engineers across Research and Development and manufacturing to design enzyme platforms, contribute to enzyme engineering efforts, and optimize processes for cost, robustness, and product quality. CRD scientists support programs from early route design and small-scale synthesis through commercial process development, pilot-scale manufacture, and technology transfer to internal and external manufacturing sites.
Boehringer IngelheimScientist IV, Drug Metabolism and Pharmacokinetics Boehringer IngelheimScientist IV, Drug Metabolism and PharmacokineticsRidgefield, CT$115,000–$181,000 / yearExperimental Medicine, BDS, CBOs, Clinical Operations, NCS Study Directors, and DMPK leads) for protocol development and review, sample handing, sample analysis plans, data transfers, milestones, report timelines, accurate budgeting, and other clinical/nonclinical requirements. Additionally, this role is responsible for the scientific monitoring and outsourcing of clinical and nonclinical bioanalytical studies, serving as the primary key contact and liason between DMPK, clinical trial teams, Nonclinical Safety, and bioanalytical CROs.
Varite, IncScientist III Varite, IncScientist IIIRidgefield, CT$49.62–$53.16 / hourEducation: Master's degree from an accredited institution with one-plus (1+) years of experience in a related scientific discipline (Computer Science, Genomics, Biostatistics or Bioinformatics preferred) OR Bachelor's degree from an accredited institution with seven-plus (7+) years of experience in a STEM discipline. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.
Bio-Techne CorpProduct Support Scientist Bio-Techne CorpProduct Support ScientistWallingford, CT$81,900–$134,550 / yearPosition Summary: We are seeking a proactive and solutions-driven Product Support Scientist to advance the performance, reliability, and customer success of our automated microfluidic-based biomarker analysis platform. This is an exciting opportunity to make a meaningful impact within a fast-paced, customer-focused organization dedicated to delivering high-quality solutions to the fluid biomarker research community.