- Guthrie (Sayre, PA)
- …a senior administrative executive to collaboratively lead the strategic, operational, and compliance functions of DGF. This role is central to ensuring the effective ... oversight responsibilities across core domains: + Clinical Research Operations in compliance and in regulatory areas. + Supports research and scholarly activities… more
- Actalent (Atlanta, GA)
- …(RN) - Infusion Experience Required Duties + Collaborate with the Principal Investigator (PI) to ensure compliance with FDA regulations, sponsor protocols, ... and GCP guidelines + Administer investigational and approved IV therapies + Screen, recruit, and consent study participants + Conduct study visits, collect data, and complete case report forms (CRFs) + Monitor and report adverse events (AEs), serious adverse… more
- Rush University Medical Center (Chicago, IL)
- …studies, single site studies, intergroup studies, industry studies, and investigator initiated studies. Prepares internal and external regulatory submissions ... group studies, single site studies, intergroup studies, industry studies, and investigator initiated studies. * Writes and prepares IRB regulatory submissions,… more
- Mayo Clinic (Rochester, MN)
- …survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and ... institutional guidelines. + May assist in complex (ie interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. + Screens, enrolls, and recruits research participants. +… more
- IQVIA (Denver City, TX)
- …done in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, codes of conduct. ... boards. + Consult with physicians, pharmacists, and other medical professionals, in compliance with relevant laws and regulations, to refer appropriate patients to… more
- J&J Family of Companies (Titusville, NJ)
- …in ensuring that investigator grants comply with overall study costs and compliance guidelines. + Comply with requests from QA and auditors. + Work proactively ... team in the pricing, planning, execution and control of site/ investigator budgets and contracts. **You will be responsible to:**...as assigned. + Adhere to SOPs, ethics and departmental compliance as determined by GD management as well as… more
- Mount Sinai Health System (New York, NY)
- …questionnaires. + Obtain informed consent under supervision of the study investigator (s); educate participants regarding study requirements. + Screen patients for ... subjects with sponsoring agency. + Coordinate research team to ensure compliance with planned treatment protocol including required laboratory and radiographic… more
- Cedars-Sinai (Beverly Hills, CA)
- …teams to develop and negotiate budgets, review contracts, and ensure compliance with institutional and sponsor regulations. This position requires strong attention ... trial budgets for industry, National Institutes of Health (NIH), and investigator -initiated clinical research. Evaluates research protocols to assess resource needs,… more
- University of Pennsylvania (Philadelphia, PA)
- …processing/handling. The CRC will demonstrate vigilance in patient safety, protocol compliance , and data quality, and will participate in data organization for ... performed, reporting adverse events and ensuring review and appropriate follow-up by investigator , monitoring patient care and treatment side effects in concert with… more
- Houston Methodist (Houston, TX)
- …patients under the supervision of the Clinical Trials Manager and Principal Investigator . This position implements clinical research patient care via the research ... institution to support and provide guidance on the administration of the GCP compliance , financial and other related aspects of the research study. This position… more