Senior Clinical Research Coordinator National InstituteSenior Clinical Research CoordinatorHuntington Beach, CaliforniaPerform or provide direct oversight of Clinical Research Coordinator responsibilities, including subject visits, informed consent, source documentation, investigational product accountability, data entry, query resolution, scheduling, specimen processing, and sponsor communication when necessary to support site operations. Additionally, you will formally supervise, support, and mentor clinical staff—including Coordinators, Principal Investigators, and Sub-Investigators—to optimize patient flow and deliver exceptional performance.
Project Manager II - PDC Advocate Health and Hospitals CorporationProject Manager II - PDCCharlotte, North Carolinaor B.S. degree in Health Administration, Engineering, Construction Management, Architecture, Business Management, Civil Engineering, or a related discipline with 2 years of experience in healthcare or academic design and construction preferred or an equivalent combination of education and experience. Providing 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.
Project Manager/Research Coordinator 3 (Temporary) University of WashingtonProject Manager/Research Coordinator 3 (Temporary)Seattle, WAThe Kidney Research Institute (KRI) has an excellent opportunity for a temporary Project Manager/Research Coordinator 3 to provide expert level lead support for multi-funded and multi-site clinical research studies involving human subjects with kidney disease and related conditions. The Kidney Research Institute functions as the research arm within the Nephrology Division of the UW Department of Medicine with a goal of conducting innovative clinical research to improve the health and quality of life of persons with renal disease and related conditions.
Clinical Research Coordinator A (Department of Cardiovascular Medicine) University of PennsylvaniaClinical Research Coordinator A (Department of Cardiovascular Medicine)Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Responsibilities will include screening records for eligibility, recruitment of study subjects, conducting study visits, data collection and entry, coordinating with study team members and external departments to successfully execute studies.
Manager, Research Early Phase Program Tennesssee OncologyManager, Research Early Phase ProgramNashville, TNWorking collaboratively with physicians, advanced practice providers, research nurses, clinical research coordinators, clinic leadership, and SOC staff, the Manager oversees patient screening workflows, monitors operational performance, coordinates multidisciplinary communication, and drives continuous process improvement. This role is responsible for identifying and tracking potential clinical trial participants, optimizing patient enrollment, maintaining program performance metrics, and leading quality and safety initiatives that support the successful execution of the Phase I Unit and other early phase oncology studies in a community oncology setting.
Manager, Clinical Data Management in a CRO Elan SolutionsManager, Clinical Data Management in a CROCaliforniaProvide data management expertise to project teams, clients, and CROs, including study startup documents, data cleaning, DCF/query tracking, database QC, and SAE/AE reconciliation. B.S./B.A. in a science or technical discipline with 8 years of data management experience, or MS degree with 6 years of data management experience; minimum 4 years in the Pharmaceutical/Biotechnology industry or CRO environment.
Sr.Clinical Data Manager Katalyst Healthcares & Life SciencesSr.Clinical Data ManagerEdison, NJPerform or provide oversight to staff for all CDM activities from study startup to archival: design CRFs/eCRFs, create Data Validation Specifications, Data Management Plans, eCRF Completion Guidelines, and Data Review Plans, code terms in MedDRA and WHO Drug; and complete data base lock, archival, and closeout activities. Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing, discrepancy management, data quality review and database close and lock procedures, CDASH and SDTM data formats.
Clinical Case Manager - AT HOME Program Caritas of AustinClinical Case Manager - AT HOME ProgramAustin, TexasEssential Duties & Responsibilities (inclusive but not exhaustive): Client Services Provide case management and advocacy for an assigned group of clients in coordination with multidisciplinary team, assuming primary responsibility for developing, implementing, evaluating, and revising goals and individualized service plans in collaboration with clients. The primary role of the Clinical Case Managers is to assess, plan, develop, coordinate, and provide therapeutic and rehabilitative services to an average case load of 17 clients with severe and persistent mental illnesses, chronic health conditions, and/or substance use disorder.
NewClinical Supervisor JobotClinical SupervisorLos Angeles, CA$105,000–$115,000 / yearKey services include housing, mental health care, medical care, domestic violence services, substance abuse treatment, income assistance and life skills programs --- all aimed at improving the self-sufficiency of the individuals and families served. Day to Day Responsibilities: Attend meetings, respond to email correspondence, develop and maintain appropriate relationships (including with the Department of Mental Health and other Intensive Case Management support organizations) on behalf of the Senior Director and staff.
Clinical Research Nurse Coordinator University of Kansas Medical CenterClinical Research Nurse CoordinatorKS$70,200–$105,300 / yearThe position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. Job Description Summary: The Clinical Research Nurse Coordinator in the Cancer Center manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
NewRN Clinical Team Lead - Intermediate Care Unit NIghts Methodist Health SystemRN Clinical Team Lead - Intermediate Care Unit NIghtsMidlothian, TXClinical Course Certifications (Basic Life Support, Advanced Cardio Life Support, Pediatric Advanced Life Support, NRP, etc.) consistent with RN requirements for specific clinical area. Providing everything from emergency care and advanced surgery to imaging and labor and delivery, our hospital has 16 emergency department beds, two operating suites, and the latest digital and medical technologies.
Clinical Manager (Menlo Park / San Mateo) US FertilityClinical Manager (Menlo Park / San Mateo)Menlo Park, California$130,000–$175,000 / yearIn this role, the Clinical Manager will: Provide leadership, management, and direction for two assigned clinic locations across all areas of local operations, including staffing, employee supervision, training and development, patient satisfaction, quality assurance, financial integrity of assigned sites, and facility appearance and maintenance. Work in close collaboration with the Executive Director, Clinical Director, and other members of the management team to promote open communication, ensure the delivery of the highest quality care to all patients, and facilitate revenue growth for the Practice.
Sr. Clinical Data Manager Artivion IncSr. Clinical Data ManagerKennesaw, GAThis includes but is not limited to database set-up (build, develop, and perform user acceptance testing), development of study documents, training, data review, query generation and resolution, and overall maintenance of study databases to ensure data integrity from study start-up to database lock. Company Overview: Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases.
Sr. Clinical Trial Manager Frontier MedicinesSr. Clinical Trial ManagerBoston, MA$125,000–$170,000 / yearDirector, Clinical Operations, you will serve as a key operational contact for our CROs and trial sites, helping drive feasibility assessments, site selection, start-up, maintenance, and close-out. This is a hybrid role based in our Boston, MA office, with an expectation of 2-3 days per week onsite, plus periodic travel to trial sites and CRO/vendor meetings as needed.
Clinical Manager (San Ramon / Oakland) US FertilityClinical Manager (San Ramon / Oakland)San Ramon, CaliforniaIn this role, the Clinical Manager will: Provide leadership, management, and direction for two assigned clinic locations across all areas of local operations, including staffing, employee supervision, training and development, patient satisfaction, quality assurance, financial integrity of assigned sites, and facility appearance and maintenance. Work in close collaboration with the Executive Director, Clinical Director, and other members of the management team to promote open communication, ensure the delivery of the highest quality care to all patients, and facilitate revenue growth for the Practice.
Clinical Research Coordinator A/B/C University of PennsylvaniaClinical Research Coordinator A/B/CPhiladelphia, PA$47,313–$70,000 / yearAs part of the Department of Medicine, the DOM Clinical Trials Unit supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.
Clinical Case Manager (CASE MGR NEX) University of CaliforniaClinical Case Manager (CASE MGR NEX)Davis, CA$75.58–$110.71 / hourCritical aspects of the role involve the assessment of clinical information to determine medical necessity for the identified level of care, assessment for appropriate services needed and resources available, and to facilitate the coordination of both internal and external health care providers to ensure optimal continuity of appropriate and cost-effective care. The Clinical Case Manager accurately maintains and tracks pertinent data and statistics specific to area of practice, such as delays in service, patients who lack medical necessity for acute hospital admission, denials for continued stays, and other factors affecting appropriate utilization of health system resources.
NewSenior Manager, Research, SOM/Pediatrics Virginia Commonwealth UniversitySenior Manager, Research, SOM/PediatricsRichmond, VA$100,000–$110,000 / yearResponsibilities include coordinating clinical trial startup, supporting initial IRB submissions, preparing sponsor reports, gathering information for complex research grants, and providing oversight of research staff responsible for accurate and timely data entry, sponsor queries, and other study requirements. The position serves as a key operational partner to Principal Investigators throughout the study lifecycle, providing guidance and direct support related to study startup, staffing, regulatory requirements, operational workflows, financial feasibility, sponsor requirements, and study performance.
NewClinical Research Coordinator A/B University of PennsylvaniaClinical Research Coordinator A/BThe job functions include: Source documentation generation in study startup; Contacting patients and caregivers to schedule research visits, Tracking enrollment progress; Organizing and coordinating research visits; Run the study visit (cognitive testing, MRI, biofluids) per protocol; Biofluid collection, processing, and shipping per protocol; Maintain records of monthly/yearly progress reports, protocols and ICFs tracking and version control in shared drive, Maintain source documentation of study activities, including essential document and correspondence; Invoice study activities, Perform subject reimbursement according to study protocol and verify accuracy; Perform data entry; Performing preliminary cognitive or imaging analyses if applicable. Applicants with prior experience with federally funded clinical research, multi-site research studies, early onset neurodegenerative disease, relevant regulations for the conduct of clinical research including Title 21 Code of Federal Regulations (CFR), International Conference of Harmonization (ICH) Guidelines, etc. are preferred.
Sr. Program Manager, Clinical Chemistry & Immunoassay (Business Unit) DanaherSr. Program Manager, Clinical Chemistry & Immunoassay (Business Unit)Chaska, Minnesota$160,000–$175,000 / yearLead, mentor and develop high-performing teams through shared purpose and project goals—leveraging advanced leadership, communication, influence, cross-cultural awareness, negotiation, and conflict resolution skills to consistently meet objectives. Drive high-impact, business-critical programs utilizing Danaher Business System (DBS) tools and methodologies to ensure operational excellence in efficiency, quality, budget, schedule and resource optimization to achieve Quality, Cost, and Delivery (QCD) objectives.