Clinical Trials Project Manager Yale UniversityClinical Trials Project ManagerConnecticutRemoteThe Clinical Trials Project Manager provides sponsor level project management and operational leadership for investigator-initiated clinical trials (IITs) and clinical trials conducted through the NCI Experimental Therapeutics Clinical Trials Network (ETCTN) for which the institution and/or investigator has sponsor, coordinating center, or National Principal Investigator responsibilities. The Project Manager partners closely with Principal Investigators, Clinical Research Managers, regulatory and clinical operations teams, contracting and finance, pre-award, laboratories, external vendors and funders, and participating institutions to move studies from concept and feasibility through activation, conduct, closeout, and required reporting.
AD/Sr. AD, Market Research & Competitive Intelligence - Rheumatology Boehringer IngelheimAD/Sr. AD, Market Research & Competitive Intelligence - RheumatologyRidgefield, CT$170,000–$269,000 / yearEight (8) to ten plus (10+) years´ experience in Pharma Industry with a working knowledge of drug development process, including activities from pre-clinical through marketing of a product, anatomy and physiology and principles of disease, rationale for treatment algorithms and business knowledge of pharma companies and their business practices. + Primary responsibility for all aspect of CI for specific TA/brand including the identification of knowledge gaps, the development of brand aligned KITS/KIQs, the leveraging of appropriate CI methodologies to fill the intel gaps and the clear communication of the intelligence and related implications and insights for our strategic brands.
Sr 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.
MRI Research Technologist Yale UniversityMRI Research TechnologistNew Haven, CTHealthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. Required Education and Experience Six years of related work experience, four of them in the same job family at the next lower level, and high school level education; or four years of related work experience and an Associate's degree, or little or no work experience and a Bachelor's degree in a related field; or an equivalent combination of experience and education.
Oncology Research Regulatory Coordinator Trinity Health CorporationOncology Research Regulatory CoordinatorHartford, CTDescription: The Oncology Research Regulatory Coordinator (RC) reports to the Oncology Clinical Research Manager and is responsible for coordinating regulatory activities for clinical research studies. This role supports protocol submissions, regulatory document preparation, and maintenance of study records to ensure compliance with Trinity Health Of New England policies, federal regulations, and ICH/GCP guidelines.
Research Finance Specialist - Oncology Trinity Health CorporationResearch Finance Specialist - OncologyHartford, CTThe Research Finance & Billing Compliance Specialist serves as a key partner to investigators, research coordinators, finance teams, and operational stakeholders by overseeing clinical trial budgeting, research billing compliance, payment reconciliation, grant financial management, and research-related financial reporting. As part of our Oncology Clinical Research team, you will play a meaningful role in supporting groundbreaking cancer research and helping bring new treatment options to patients throughout our communities.
YCCI Clinical Trials Project Specialist Yale UniversityYCCI Clinical Trials Project SpecialistNew Haven, CT$61,500–$91,875 / yearThe role supports a culture appropriate for a large physician organization with clinical affiliations across multiple academic and non-academic medical centers including assisting in coordinating initiatives which identify, prevent, and appropriately mitigate multisite trials and FDA 21 CFR Part 11 research system compliance risk, support efforts to ensure YSM, YM, YNHH compliance efforts align with the university's broader compliance strategy and framework. The position works effectively with other team members and units/departments within the university such as biostats (YCAS), EHR research team (JDAT), Human Subjects Protections (HRPP), industry contracting team, and finance; clinical trials sponsors and vendors; and with research teams at other academic centers.
Ycci Clinical Trials Project Specialist Yale UniversityYcci Clinical Trials Project SpecialistNew Haven, CT$61,500–$91,875 / yearThe role supports a culture appropriate for a large physician organization with clinical affiliations across multiple academic and non-academic medical centers including assisting in coordinating initiatives which identify, prevent, and appropriately mitigate multisite trials and FDA 21 CFR Part 11 research system compliance risk, support efforts to ensure YSM, YM, YNHH compliance efforts align with the university's broader compliance strategy and framework. The position works effectively with other team members and units/departments within the university such as biostats (YCAS), EHR research team (JDAT), Human Subjects Protections (HRPP), industry contracting team, and finance; clinical trials sponsors and vendors; and with research teams at other academic centers.
Administrative Assistant - Research Support Services The Jackson LaboratoryAdministrative Assistant - Research Support ServicesFarmington, Connecticut$22.04–$28.65 / hourActs as a liaison between assigned Staff and the Scientific Director's Office, Office of Sponsored Research Administration and other administrative areas of the institution, as well as applicable administrative areas of external organizations often serve as the first point of contact for visitors, collaborators, and job candidates. Liaises with the Office of Sponsored Research Administration and Research Program Development to assist with documents for grant submissions including faculty and research staff bio sketches/CV, letters of support, documents for compliance reporting, progress reports, and others as required by the granting agency.
Patent Agent - Research The Jackson LaboratoryPatent Agent - ResearchFarmington, CT$106,020–$153,729 / yearAbout JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Provide Sponsored Research Administration with patent filing data for annual progress reports, renewal applications, award closeouts, and final invention statements reported in iEdison under the Bayh-Dole Act.
Account Manager -Biotech, Business Development - Clinical Trials Division Thermo Fisher Scientific IncAccount Manager -Biotech, Business Development - Clinical Trials DivisionCTNew Business Development including identifying new molecule opportunities with new or existing clients through understanding of the market, appointment based strategic selling, leveraging personal network, interaction with other Pharma Services Group (PSG), Clinical Research Group (CRG) and Thermo Fisher Scientific teams, and following up on leads. With more than 65 locations globally, we provide our clients with integrated, end-to-end capabilities through all phases of development, including API, biologics, viral vector services, formulation, clinical trial solutions, logistics services and commercial manufacturing.
Clinical Affairs Scientist Agilent Technologies IncClinical Affairs ScientistCT$105,280–$197,400 / yearThe candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.
Scientific Research Associate VIRSCIO, INC.Scientific Research AssociateNew Haven, CTThe Scientific Research Associate will work across Virscio to review study protocols, support and set up study specific electronic data capture systems (Provantis, Excel, Word), manage study scheduling, pull out and organize data to enable downstream analysis, QC draft reports, and draft SOPS and report templates. Experience working with Anatomic Pathology electronic data capture modules (Provantis, Concentriq, Visiopharm, etc.) including setting up individual studies, generating reports and tabulated data.
NewAssociate Clinical Experience (ACE) Intern - Summer 2027 Medtronic PlcAssociate Clinical Experience (ACE) Intern - Summer 2027CTThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Senior Research Fellow - Project Toxicologist, Neuroscience and Eye Health Boehringer Ingelheim International GmbHSenior Research Fellow - Project Toxicologist, Neuroscience and Eye HealthRidgefield, CT$166,600–$250,000 / yearSupport the implementation of scientifically robust non-clinical safety strategies, spanning from NTC discovery through clinical trial execution to regulatory submission for marketing authorization, specifically for the development of intravitreal (IVT) medications in eye health across various modalities, ensuring alignment with external requirements and benchmark project strategies. Your role includes advising on all aspects of nonclinical safety for new drugs of different Modalities-covering the nonclinical testing strategy, study design, dose selection, and the overall toxicological assessments-and supporting the preparation of development plans, protocols, reports, and regulatory documents.
Senior Manager, Synthetic Research & Platform Growth CVS Health CorpSenior Manager, Synthetic Research & Platform GrowthHartford, CT$82,940–$182,549 / yearThe Senior Manager will be responsible for building and operationalizing research programs, developing AI-powered customer intelligence assets, managing client engagement activities, and identifying opportunities to expand synthetic research and simulation adoption across additional business units and external partners. Position Summary: CVS Health is seeking a strategic and execution-focused Senior Manager, Synthetic Research & Platform Growth to lead the deployment, scaling, and commercialization of synthetic customer research primarily focused on third-party research delivery.
Research Programmer University of PennsylvaniaResearch ProgrammerNew Haven, CT$61,000–$73,581 / yearLong-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Preferred: Experience with biological or biomedical data (genomic, transcriptomic, or clinical); familiarity with SQL or NoSQL databases; experience with data visualization libraries (e.g., Plotly, Dash, Tableau).
Sr. AD, Market Research & Competitive Intelligence - Rheumatology Boehringer Ingelheim International GmbHSr. AD, Market Research & Competitive Intelligence - RheumatologyRidgefield, CT$170,000–$269,000 / yearEight (8) to ten plus (10+) years´ experience in Pharma Industry with a working knowledge of drug development process, including activities from pre-clinical through marketing of a product, anatomy and physiology and principles of disease, rationale for treatment algorithms and business knowledge of pharma companies and their business practices. Primary responsibility for all aspect of CI for specific TA/brand including the identification of knowledge gaps, the development of brand aligned KITS/KIQs, the leveraging of appropriate CI methodologies to fill the intel gaps and the clear communication of the intelligence and related implications and insights for our strategic brands.
NewClinical Technologist 1, Dermatology, Dermatopathology Yale UniversityClinical Technologist 1, Dermatology, DermatopathologyNew Haven, CTUnder the supervision of the Laboratory Manager and with a thorough knowledge and understanding of clinical laboratory support functions, techniques, processes to ensure excellent patient care services and research support initiatives. Required Education and Experience Four years of related work experience, two of them in the same job family at the next lower level, and a high school level education; or two years of related work experience and an Associate''s degree; or an equivalent combination of experience and education.
Director of Research, Weitzman Institute-Remote Community Health Center IncDirector of Research, Weitzman Institute-RemoteCTRemoteThe ideal candidate will be an accomplished research leader with a demonstrated record of building externally funded research programs, producing high-impact scholarship, developing and mentoring high-performing teams, cultivating strategic partnerships, and translating evidence into practice and policy. The Director of Research position affords a rare research environment: direct access to real-world clinical and EHR data, established pathways to patients, providers, and community partners in the safety net, and the ability to move from study design through implementation and dissemination within a large integrated health system, translating evidence into practice and policy at national scale.