Clinical Research Associate Allen SpoldenClinical Research AssociateNew York, New JerseyConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Associate II Allen SpoldenClinical Research Associate IIColumbus, ArkansasConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Associate II Katalyst Healthcares & Life SciencesClinical Research Associate IIremote, NJRemoteResponsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary.
Clinical Research Assistant Temple UniversityClinical Research AssistantPhiladelphia, Pennsylvania$45,000The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.
NewResearch Scientist – Physiologist/Biomedical Engineer LeidosResearch Scientist – Physiologist/Biomedical EngineerGroton, CT$87,100–$157,450The Defense Health Operation of Leidos is currently looking for a Research Physiologist/ Biomedical Engineer to support research in the areas of physiology and biomedical engineering as it may pertain to warfighters operating in extreme or austere environments at the Naval Submarine Medical Research Laboratory (NSMRL) in Groton, CT. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com .
Clinical Research Nurse/Coordinator US Oncology IncClinical Research Nurse/CoordinatorVACookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
NewRemote Clinical Research Data Coordinator II - Dallas, Tx US Oncology IncRemote Clinical Research Data Coordinator II - Dallas, TxDallas, TXRemoteCookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
Oncology Clinical Research Nurse/Coordinator US Oncology IncOncology Clinical Research Nurse/CoordinatorVACookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
NewManager Clinical Research Cone HealthManager Clinical ResearchOversees the fiscal operations of the department, including preparing and managing departmental and pharmaceutical studies budgets, ensuring financial accountability and efficient resource allocation to support the successful execution of research projects. The Manager Clinical Research manages team members that work closely with study subjects and other research staff and supervises most steps of the research trial process to collect, compile, document, and analyze clinical research data.
Clinical Research Coord 3, Mcvi Research, FT, 8A-4:30P Baptist Health South FloridaClinical Research Coord 3, Mcvi Research, FT, 8A-4:30PMiami, FL$32.12–$41.76 / hourMust be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner. In lieu of Bachelor's degree, Associates degree with 6 years of research experience OR a Foreign Medical Degree with 2 years of experience required.
NewClinical Research Associate II National Marrow Donor ProgramClinical Research Associate IICAAdditionally, this position is responsible for coordinating and providing support for all aspects of the study including protocol and site management, providing training to junior team members, and demonstrates comprehensive knowledge of the monitoring functions. May serve as Lead CRA on studies with multiple assigned CRAs, including developing and monitoring of study metrics, overseeing clinical monitoring plan compliance and escalating study risk, with supervision.
Senior Clinical Research Associate - East Coast ICON PlcSenior Clinical Research Associate - East CoastBlue Bell, PAICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate II RQM+Clinical Research Associate II$90,000–$97,000 / yearOur tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better. Behaviors: Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning.
Clinical Research Coordinator Northwestern Memorial HealthCareClinical Research CoordinatorILMaintains research files, designs forms as needed, reports findings as appropriate, assists in preparation or review of material for submission to an IRB including reviewing and editing protocols and consent documents, where applicable. Attends investigator's meetings, coordinates and attends pre-study site visits, study initiation visits, and all other study-related visits by Monitors or Sponsor representatives, when required.
Clinical Research Coordinator CRC II NATIONAL CLINICAL TRIALS INCClinical Research Coordinator CRC IILos Angeles, CAFull timeNational Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA, dedicated to advancing healthcare through innovative and rigorous clinical studies. In this role, you'll play a critical part in advancing medical research by coordinating and managing clinical trials that make a real difference in patients' lives.
Clinical Research Coordinator Eye Associates of New MexicoClinical Research CoordinatorAlbuquerque, NMIf you are detail-oriented, passionate about advancing patient care through clinical research, and enjoy working in a collaborative healthcare environment, we encourage you to apply. Skills/Requirements: Prior clinical research experience or Certified Clinical Research Coordinator (CCRC) certification preferred.
NewClinical Research Coordinator - On Site Only Great Plains HealthClinical Research Coordinator - On Site OnlyNorth Platte, NebraskaMinimum Qualifications o Education o Associates degree from a two year college or technical school (nursing, pharmaceutical or science related field) and six months experience in related medical fields preferred OR A general Associates degree and 1 year of direct responsibility for clinical research or one year as an Assistant Research Coordinator (ARC) o Credentials o State Required: None o GPRMC Preferred: None Physical Demands 1. Participates in an array of tasks associated with clinical research to include: collection of data in an organized and timely fashion while promoting and upholding attitudes of caring, compassion, justice and respect for the human person.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedCarlsbad, CA$71,900–$189,000 / yearPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Ensure 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.
Senior Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncSenior Clinical Research Associate, Sponsor DedicatedOverland Park, KS$74,500–$197,500 / 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 Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedCarlsbad, CA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.