Clinical Research Coord Assoc University of MichiganClinical Research Coord AssocBrighton, MIThis position will serve as a Clinical Research Coordinator Associate in the Oncology Clinical Trial Support Unit (O-CTSU) - Clinic Research Group located in the Brighton Center for Specialty Care providing study coordination support to faculty and research teams for the University of Michigan Rogel Cancer Center - an NCI-Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN). It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate e-clinical technologies with a reasonable degree of proficiency.
Nurse Practitioner / Physician Assistant (Weekend Clinical Research) HealthOp SolutionsNurse Practitioner / Physician Assistant (Weekend Clinical Research)Chandler, AZRemote$130,000–$155,000 / yearThis is a specialized opportunity for an APP who understands clinical research and wants direct involvement in the evaluation of emerging therapies while providing high-quality care to patients with liver and gastrointestinal conditions. Your responsibilities will include understanding assigned protocols, completing research visits, reviewing source documentation and informed consent records, and ensuring clinical decisions align with patient safety and study requirements.
Clinical Research Coordinator III Tulane UniversityClinical Research Coordinator IIILafayette, LAPreferred Qualification: Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired. The Clinical Research Coordinator III screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive tests according to study protocols.
Clinical Research Manager, Research Incubation Unit University of ChicagoClinical Research Manager, Research Incubation UnitChicago, IL$90,000–$130,000 / yearThe Clinical Research Incubation Unit was established to enable growth of clinical research portfolios across the Biological Sciences Division as well as provide timely research staffing services to departments or units in need of short-term clinical research management services. The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.
Clinical Research SupervisorCoordinator - Pediatrics UCLA Health SystemClinical Research SupervisorCoordinator - PediatricsLos Angeles, CA$88,900–$190,300 / yearThe Department of Pediatrics Clinical Research Excellence at Work (CREW) Clinical Research Coordinator Supervisor is an experienced professional responsible for overseeing, coordinating, and managing complex investigational drug clinical trials, as well as supervising other clinical research coordinators. Demonstrated interpersonal and communication skills to work with patients, their families/ guardians, physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Clinical Research Director Southwest Womens Oncology/OptimumClinical Research DirectorAlbuquerque, NMFull timeYou will work at the intersection of scientific rigor, operational excellence, and patient impact, partnering with:Gynecologic oncology physicians serving as Principal InvestigatorsPharmaceutical sponsors, CROs, and cooperative group partnersClinical Research Coordinators, data specialists, and research support staffExecutive leadership and the broader Optimum platformRegulatory bodies including FDA, NIH, and IRBYou will have the authority, the resources, and the leadership support to build a program that changes what's possible for patients in New Mexico and beyond. What You'll OwnStrategy & Program LeadershipBuild, scale, and manage the clinical research vertical within SWWO, developing long-term strategy, infrastructure, and resourcing plans.
Regulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levels University of VirginiaRegulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levelsCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginia's (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. This position is open to applicants who meet the requirements of Clinical Research Coordinator 2, 3 and 4. The CRC will work closely with physicians, research staff, sponsors, IRB and regulatory department staff.
Clinical Research Coordinator, Varying Levels; Cardiovascular Medicine University of VirginiaClinical Research Coordinator, Varying Levels; Cardiovascular MedicineCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginia's (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. Research reference information: Innovating proctoring with live/recorded surgical cases, spanning across departments: https://www.uvaphysicianresource.com/uva-structural-heart-disease-team-performs-live-cases-at-the-2021-international-tvt-conference/ .
Sr. Clinical Research Nurse - Transplant Center Houston MethodistSr. Clinical Research Nurse - Transplant CenterTexasAssists Principal Investigator to ensure that all persons ‘engaged’ in research studies have met training requirements in accordance with Federal regulations and entity policies and procedures including preparing Institutional Review Board (IRB) and regulatory documents following ICH/GCP guidelines, and the development of materials and tools necessary to appropriately facilitate the conduct of research. Leads initiatives to improve quality and safety scores, through peer-to-peer accountability Performs nursing functions independently while following the clinical research protocol and nursing process which would include, modification of care based on continuous evaluation of the research patient’s condition.
Clinical Research Administrator - Pediatrics TMC University of Texas Health Science Center at HoustonClinical Research Administrator - Pediatrics TMCHouston, TXCertification/Skills: NoneMinimum Education:Bachelor''s Degree in Healthcare Administration, Business, Finance, Accounting, or related degree requiredMinimum Experience:3 years of related experience requiredPhysical Requirements:Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Clinical Research Assistant - OLOL FMOL HealthClinical Research Assistant - OLOLBaton Rouge, LAUnder the direct supervision of the Clinical Research Manager and the Principal Investigator (PI), the Research Assistant is responsible for the coordination and implementation of assigned research projects, data management, and communication of protocol activity within the Office of Research. Collaborates with PI and Clinical Research Manager to develop materials and tools necessary to appropriately train key personnel in the protocol requirements, schedule of visits, and execution of clinical trial agreement.
NewClinical Research Coordinator Associate underfill Technician or Assistant University of MichiganClinical Research Coordinator Associate underfill Technician or AssistantAnn Arbor, MICertification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates should be able (or willing to develop the ability) to perform most tasks independently, conduct quality checks of their own work, identify and use appropriate resources and support, and recognize when to escalate issues requiring additional intervention.
Medical Director Oncology Clinical Research Hematology & Oncology Physician The Oncology Institute of Hope and InnovationMedical Director Oncology Clinical Research Hematology & Oncology PhysicianLas Vegas, NVWorking closely with Starling Oncology's Chief Medical Officer, physicians, clinical research coordinators, and research operations teams, the Medical Director will provide physician leadership for our clinical research program, expand patient access to clinical trials, strengthen Principal Investigator oversight, and help identify the trials that can have the greatest impact for the communities we serve. Formerly known as The Oncology Institute, Starling Oncology offers cutting-edge, evidence-based cancer care to a population of approximately 2.1 million patients, including clinical trials, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations.
Medical Director Oncology Clinical Research Hematology & Oncology Physician Starling OncologyMedical Director Oncology Clinical Research Hematology & Oncology PhysicianLas Vegas, NVWorking closely with Starling Oncology's Chief Medical Officer, physicians, clinical research coordinators, and research operations teams, the Medical Director will provide physician leadership for our clinical research program, expand patient access to clinical trials, strengthen Principal Investigator oversight, and help identify the trials that can have the greatest impact for the communities we serve. Formerly known as The Oncology Institute, Starling Oncology offers cutting-edge, evidence-based cancer care to a population of approximately 2.1 million patients, including clinical trials, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations.
Administrative Director, Clinical Research Operations University of RochesterAdministrative Director, Clinical Research OperationsOversee the financial performance of clinical trial operations, including budgeting, forecasting, and resource allocation and report financial performance and portfolio growth metrics to cancer center leadership and relevant oversight committees, Identify opportunities to improve operational efficiency, optimize cost structures, and enhance revenue generation through research activities. In collaboration with the Associate Director for Clinical Research, Associate Director for Administration, and the Clinical Trials Office (CTO) Medical Director, the incumbent will ensure the development of WCI’s clinical research infrastructure is consistent with expectations of NCI-designated Cancer Centers as outlined in the Cancer Center Support Grant (CCSG) guidelines.
Clinical Operations Manager Tessera TherapeuticsClinical Operations ManagerSomerville, MA$164,000–$199,000 / yearYou have previously demonstrated ability to partner with and proactively manage internal stakeholders, CROs, and vendors, and collaborate cross-functionally to deliver global clinical trials according to the planned timelines and budget, while ensuring quality in accordance with ICH-GCP guidelines and regulatory requirements. Bachelor's degree in a relevant scientific or healthcare discipline, with 8+ years of clinical operations experience, including 4+ years as a clinical trial manager, leading cross-functional teams and accountable for planning and executing global clinical trials.
NewVice President, Emory Clinical Research Office (ECRO) Emory UniversityVice President, Emory Clinical Research Office (ECRO)Atlanta, GAReporting to the Associate Chief Scientific Officer, the Vice President is responsible for the strategic, operational, and financial leadership of ECRO, including pre- and post-award administration, grants and contracts management, clinical research compliance and transparency, and operational support services designed to meet the needs of Emory''s world-class investigators as they pursue groundbreaking clinical research. ECRO provides integrated clinical research administration services, in partnership with other Emory University offices, schools, and units, across a broad and diverse portfolio of industry-sponsored, federally funded and other non-industry-sponsored clinical research, encompassing more than 1,000 active clinical studies.
Vice President, Clinical Development Grifols SAVice President, Clinical DevelopmentNCWith responsibility across a diverse therapeutic portfolio and modalities - including plasma-derived products and recombinant proteins - this role offers a rare opportunity to build future-ready development capabilities, influence portfolio strategy, and lead teams that translate deep biological insight into medicines that meaningfully improve patients' lives. Author and deliver high-quality clinical regulatory documents: Lead the planning, writing, and review of key documents including clinical study reports (CSRs), protocols, investigator brochures, briefing packages, and regulatory submissions, ensuring clarity, scientific rigor, and compliance with ICH/GCP and regulatory guidelines.
Clinical Research Monitor II Temple University Health SystemClinical Research Monitor IIPhiladelphia, PA404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true'',''Clinical Research Monitor II'',''263138'',''!*!The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research & Science'',''Research & Science'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''404810'',''404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true''.
Virtual Health-Sleep Specialty- Full-Time- NP/PA Advocate Health and Hospitals CorporationVirtual Health-Sleep Specialty- Full-Time- NP/PACharlotte, North CarolinaProviding care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.