- Actalent (Fairfax, VA)
- …procedures to collect data on patients enrolled or seeking enrollment in clinical studies . Responsibilities + Verify and correct research study information on ... feedback to the site data collector. + Input research study data into the trial Electronic Data Capture system,...content accuracy and completeness. + Prepare and maintain research study files and compile, collate, and submit study… more
- Actalent (Omaha, NE)
- …You will play a critical role in coordinating clinical research studies , ensuring compliance with regulations, and maintaining high ethical standards. Key ... + Develop strong working relationships and maintain effective communication with study team members. + Coordinate day-to-day activities of research visits, including… more
- Johns Hopkins University (Baltimore, MD)
- …for supporting complex quantitative and data modeling research projects in ongoing studies addressing violence and mental health comorbidities among Black women and ... organizations. + Collaborate with PI on protocol development and study design. + Develop, or oversee development of standard...regulatory compliance issues. + Develop, or oversee development of, study budget(s) and ensure that all study … more
- Dana-Farber Cancer Institute (Brookline, MA)
- …for all studies and funding sources, as applicable. + Monitors study payment activity and consistently pursues collections from extramural research sponsors and ... Medical School-affiliated hospitals. **Primary Duties and Responsibilities:** + Submits study financial account creation requests for each new Clinical Research… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study -related documents to create a coverage analysis/billing guide. The coverage ... billable to patient insurance and which should be billed to the study sponsor.The Medicare Coverage Analyst determines whether proposed clinical research studies… more
- Parexel (Baltimore, MD)
- …the Early Phase Clinical Unit (EPCU). + Assume responsibility for patient care and study conduct assignments. + Ensure that all study laboratory and medical ... completed, and that eligibility requirements specific to the assigned study are met. Assess compliance, symptoms, etc. per ...Act as participant advocate in the conduct of clinical studies . **Qualifications** + At least 2 years working in… more
- Rush University Medical Center (Chicago, IL)
- …bills.). 10. Monitor and formulate revenue earned for work performed on research studies . 11. Perform monthly reconciliations of study financial accounts. 12. ... for interpreting agreed upon coverage analyses into a research study budget. 5. Serves as resource determining research price...as resource determining research price rates for clinical trial study budgets. Sets up study billing forms… more
- Bristol Myers Squibb (Princeton, NJ)
- …on functional area activities during program implementation, clinical study start-up/execution/close out, data analysis/reporting, and potentially support of ... trial design to develop or oversee development of specific study concept synopses and protocols. + Participates in protocol...with team members to ensure scientific integrity of clinical studies . + May be sought out for advice by… more
- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... CORE JOB FUNCTIONS + Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.… more
- Cedars-Sinai (Beverly Hills, CA)
- …Description** The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more