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.
RN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care Unit UNC HealthRN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care UnitChapel Hill, NC$33.88–$47.91 / hourOur patient populations require close post-operative observation, occasional remote cardiac telemetry, early aggressive mobilization, pulmonary hygiene, extensive physical therapies, IV, central line/PICC line care, administration of TPN, anticoagulation, oxygen therapy, pain management, blood product administration, intake/output and ostomy care. Our interdisciplinary team provides evidence-based and high-quality care primarily to adult post-surgical patients with weight loss issue, gastrointestinal (GI) cancers, and complex non-cancer GI-related illnesses.
Oncology Research Data Specialist, Canton Northside Hospital Inc.Oncology Research Data Specialist, CantonCanton, GeorgiaFull timeThe RDS works closely with the Clinical Research Nurses (CRN) and Clinical Research Coordinators (CRC) to complete all data-related tasks. If not Certified Clinical Research Professional (CCRP) at time of hire , must achieve professional certification through Society of Clinical Research Associates (SOCRA) by deadline assigned to specific work location.
Cardiology Research Data Specialist, Gwinnett Hub Northside Hospital Inc.Cardiology Research Data Specialist, Gwinnett HubLawrenceville, GeorgiaFull timeQualifications: KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION REQUIRED Associates Degree from an accredited college or university KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION PREFERRED Bachelor of Arts or Bachelor of Science degree from an accredited college or university in a data driven research - related field (such as allied health, biological sciences, chemistry, economics, mathematics, psychology, sociology, demography, geography, anthropology, statistics, data science). The RDS works closely with the Clinical Research Nurses (CRN) and Clinical Research Coordinators (CRC) to complete all data-related tasks.
Clinical Research Associate - Part Time Saint Peter's Healthcare System IncClinical Research Associate - Part TimeNew Brunswick, NJMaintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
NewPrescreen Coordinator K2 Staffing LLCPrescreen CoordinatorOcala, FLAs a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. At K2 Medical Research, people come first and we're seeking warm, wonderful humans who effortlessly click with everyone, from our incredible patients to brilliant physicians and dedicated research staff.