NewClinical Director of Adult Medicine - Physician MD/DO JobotClinical Director of Adult Medicine - Physician MD/DOHartford, CT$250,000–$325,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners.
Travel Clinical Lab Scientist (CLS) - $20 to $23 per hour in Farmington, CT job.comTravel Clinical Lab Scientist (CLS) - $20 to $23 per hour in Farmington, CTFarmington, CT$20–$23Assess and record details of animal shipments (ID, weight, health). Collect and report data on animal facility operations.
Operations Director, Clinical Laboratory Operations - Clinical Laboratory Administration - Tri State Area (New York, New Jersey, Connecticut) - Full Time/Day Shift Mount Sinai Health SystemOperations Director, Clinical Laboratory Operations - Clinical Laboratory Administration - Tri State Area (New York, New Jersey, Connecticut) - Full Time/Day ShiftHartford, CTMount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology.
Clinical Research Manager - Oncology Trinity HealthClinical Research Manager - OncologyHartford, CTAs a key liaison between research teams and organizational leadership, the Clinical Research Manager drives operational excellence across the research lifecycle, from study feasibility and startup through study conduct, quality assurance, and closeout activities. The successful candidate will provide leadership to research staff, foster strategic partnerships with sponsors and stakeholders, and support a culture of innovation, compliance, and continuous improvement.
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsSpringfield, MA$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Clinical Instructor-Coordinator of Clinical Placements University of ConnecticutClinical Instructor-Coordinator of Clinical PlacementsStorrs, CTMasters degree in nursing; Current Connecticut multistate compact RN license (valid as of date of hire, which must be maintained; Three or more years of experience teaching undergraduate students in clinical settings; Experience evaluating student performance in clinical training settings; Experience developing effective working relationships with hospitals, clinics, and other community partners; Experience evaluating preceptor performance, including in settings outside one's own area of clinical expertise; Completion of required health indicators (MMR titers, TB status, Hepatitis B, and others as required by clinical agencies) and CPR certification at the time of employment; Demonstrated communication skills and interpersonal relationship strategies. Please apply online at Faculty and Staff Positions, Search #499795 and submit the following application materials: Cover letter specifically addressing your credentials relative to the minimum and preferred qualifications listed above; Curriculum vitae; Teaching statement (including teaching philosophy, teaching experience, commitment to effective learning, concepts for new course development, etc.); Commitment to diversity statement (including broadening participation, integrating multicultural experiences in instruction and research and pedagogical techniques to meet the needs of diverse learning styles, etc.); Contact information for three (3) letters of reference.
Clinical Instructor-Coordinator of Clinical Placements UConn CareersClinical Instructor-Coordinator of Clinical PlacementsStorrs, ConnecticutAssists in the coordination of clinical placements of pre-licensure students in clinical rotations throughout the year in collaboration with the Director of Prelicensure Clinical Education and course coordinators, specifically managing student and faculty onboarding with clinical agencies, communication between students and sites, and clinical data management processes. The individual who assumes this position will also: recruit qualified people to join UConn SON faculty to serve as clinical preceptors; expand clinical placement sites in Connecticut; match available faculty to clinical sites; provide support to clinical preceptors; and participate in orientation for new faculty/preceptors.
Clinical Research Manager - Oncology Trinity Health CorporationClinical Research Manager - OncologyHartford, CTAs a key liaison between research teams and organizational leadership, the Clinical Research Manager drives operational excellence across the research lifecycle, from study feasibility and startup through study conduct, quality assurance, and closeout activities. The successful candidate will provide leadership to research staff, foster strategic partnerships with sponsors and stakeholders, and support a culture of innovation, compliance, and continuous improvement.
Pharmacy Clinical Pharmacist- Clinical Program Senior Advisor (Multiple Locations) The Cigna GroupPharmacy Clinical Pharmacist- Clinical Program Senior Advisor (Multiple Locations)Bloomfield, CT$116,200–$193,600 / yearRole Summary: This position is responsible for the development of formulary strategies involving both pharmacy and medical products, clinical actions following release of new/existing drug products, evaluating and managing drug utilization review, and pipeline product tracking and forecasting. The position works closely with matrix partners across the medical organization, PBM partners, Contracting, Pharmacy pricing/finance, Clinical Operations, Coverage Policy Unit, Pharmacy and Medical client facing partners, Pharmacy product, Analytics, Compliance, Legal, and Specialty Pharmacy.
NewPharmacy Clinical Pharmacist- Clinical Program Senior Advisor (Multiple Locations) CignaPharmacy Clinical Pharmacist- Clinical Program Senior Advisor (Multiple Locations)Bloomfield, CT$116,200–$193,600 / yearRole Summary: This position is responsible for the development of formulary strategies involving both pharmacy and medical products, clinical actions following release of new/existing drug products, evaluating and managing drug utilization review, and pipeline product tracking and forecasting. The position works closely with matrix partners across the medical organization, PBM partners, Contracting, Pharmacy pricing/finance, Clinical Operations, Coverage Policy Unit, Pharmacy and Medical client facing partners, Pharmacy product, Analytics, Compliance, Legal, and Specialty Pharmacy.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsHartford, CT$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Supv Clinical Documentation / HIM Clinical Document Mgmt Hartford HealthCare CorpSupv Clinical Documentation / HIM Clinical Document MgmtFarmington, CTResponsible for regional/facility accurate Case Mix Index (CMI), mortality observed to expected ratio (O:E), capture of appropriate severity of illness (SOI) and risk of mortality (ROM), risk adjustment and hierarchal condition capture (HCC) codes and other high quality documentation outcome measures. The Clinical Documentation Supervisor will work in collaboration with the clinical documentation specialists (CDS), coding professionals, physicians, nursing staff and other patient care givers to ensure accurate and timely clinical documentation in the medical record.
NewClinical Research Coordinator Trusted Medical PLLCClinical Research CoordinatorMiddletown,, CTTrusted Medical is seeking an experienced Clinical Research Coordinator to support our growing national clinical research program serving Veterans, active-duty military personnel, and communities nationwide. Strong team player with the ability to collaborate effectively with clinical teams, Veterans, military personnel, sponsors, vendors, and leadership .
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.
Senior Manager, Clinical Program Quality and Excellence (Oncology) Takeda Pharmaceutical Co LtdSenior Manager, Clinical Program Quality and Excellence (Oncology)MARemote$137,000–$215,270 / yearFacilitate investigations into significant quality issues, scientific misconduct and serious breach of GCP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities. OBJECTIVES: Provides quality assurance oversight of the global clinical research programs in Research and Development (R&D), Plasma Derived Therapy (PDT), Vaccines Business Unit (VBU), Oncology Business Unit (OBU) and Global Medical Marketed Products Development (MPD) with the overall goal of inspection readiness.
Clinical Research Data Assistant - Oncology Trinity HealthClinical Research Data Assistant - OncologyHartford, CTThe Research Data Assistant serves as a key member of the research team, collaborating closely with Clinical Research Coordinators, investigators, healthcare providers, and external sponsors to maintain data integrity throughout the lifecycle of oncology clinical trials. 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.
Clinical Research Registered Nurse - RN - Oncology Trinity HealthClinical Research Registered Nurse - RN - OncologyHartford, CTThe Clinical Research Nurse provides direct patient care related to research protocols, oversees study implementation and regulatory activities, and contributes to the successful execution of clinical trials that support Trinity Health's mission of serving communities through compassionate, evidence-based care. The ideal candidate combines strong clinical nursing expertise with research knowledge, exceptional organizational skills, attention to detail, and the ability to manage multiple complex projects in a collaborative healthcare environment.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedSpringfield, MA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Coordinator II - Biospecimen Hartford HealthCare CorpClinical Research Coordinator II - BiospecimenHartford, CTConduct studies in accordance with federal regulation and guidelines governing clinical research including informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring; processing, storing and shipping of research specimens in accordance with study laboratory manual and IATA regulations. In compliance with all regulatory, institutional and departmental requirements performs patient screening, consent, data collection and data entry for research protocols, and projects within Hartford Healthcare Cancer Institute.
Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Metabolic - US Any RegionCTWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.