FSP Clinical Research Associate 2 Fortrea IncFSP Clinical Research Associate 2CTRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceCTTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedCTTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
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.
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 .
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 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.
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 Research Data Assistant - Oncology Trinity Health CorporationClinical 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.
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.
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 Registered Nurse - RN - Oncology Trinity Health CorporationClinical Research Registered Nurse - RN - OncologyHartford, CTThis relationship combines Dana-Farber's nationally recognized oncology expertise with Trinity Health Of New England's commitment to delivering exceptional, locally led care close to home. In this position, you will coordinate oncology research studies, collaborate with physicians and research teams, monitor patient safety, manage regulatory documentation, and support participants throughout the clinical trial process.
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.
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.
Associate Director, Clinical Program Quality and Excellence (Oncology) Takeda Pharmaceutical Co LtdAssociate Director, Clinical Program Quality and Excellence (Oncology)MARemote$154,400–$242,550 / yearOBJECTIVES: 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. Lead 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.
Research Nurse - Danbury, Connecticut (Per Diem) Syneos HealthResearch Nurse - Danbury, Connecticut (Per Diem)ConnecticutFully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs. Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.
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.
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.
Director, Clinical Operations, Oncology Takeda Pharmaceutical Co LtdDirector, Clinical Operations, OncologyMARemote$177,000–$278,080 / yearOversight of Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities assigned to a Strategic Partner/CRO/vendor for assigned program(s), including escalation of issues to and participation in governance committees; accountable for operational risk management strategy in collaboration with Strategic Partners. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
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.