- MD Anderson Cancer Center (Houston, TX)
- …of operations and budget issues in collaboration with the principal investigator or study sponsor. Cost Analysis Provide leadership for a multidisciplinary ... verbally and in writing, as needed or as requested by the principal investigator of the study, with internal reviewers or external agencies (pharmaceutical companies… more
- University of Utah (Salt Lake City, UT)
- …control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in ... an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies. **Responsibilities** 1. Oversees compliance to… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …guidance on study development. + Liaison between the sponsor, the investigator , Winship, Emory IRBs, external IRBs and internal departments/staff. + Incumbents ... + Responsible for 35+ trial load per year of NCTN, industry and investigator -initiated trials. + Establishes and maintains processes and monitors practices to ensure… more
- Sanofi Group (Cambridge, MA)
- …colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirements + ... reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs. + Contribute to the creation of material for internal… more
- UCHealth (Loveland, CO)
- …subjects, taking vital signs, and performing electrocardiograms. + Coordinates with investigator to manage adverse events, compliance and other ... FTE: Full Time, 1.0, 80.00 hours per pay period ( 2 weeks) Shift: Days Pay: $24.11 - $36.17 /...aspects of research projects. Responsibilities: + Collaborates with principal investigator , sponsor and research staff to plan, conduct and… more
- Teva Pharmaceuticals (West Chester, PA)
- …and edits clinical regulatory documents (eg, study reports, protocols, briefing books, investigator 's brochures, health authority responses, Module 2 .5 and 2 ... experience, Lead author experience in: Protocols/protocol amendments, Clinical study reports, Investigator 's brochures, Clinical summary documents (Modules 2 .5, … more
- Mount Sinai Health System (New York, NY)
- …other assigned lab, as directed by the Laboratory Manager or Principal Investigator . **Qualifications** BS in Medical Technology or equivalent education to meet NYS ... **Responsibilities** 1. Demonstrates the ability to perform clinical/technical/service/administrative tasks. 2 . Performs technical procedures in chemistry /hematology including but… more
- Beth Israel Lahey Health (Burlington, MA)
- …implementation of all aspects of clinical trials research adhering to Research SOPs, GCP compliance and FDA regulations. 2 ) Functions as a mentor, resource and ... on a continuous basis in light of ethical considerations and protocol compliance . + Directly retrieves and/or coordinates the retrieval and submission of patient… more
- University of Pennsylvania (Philadelphia, PA)
- …research protocols, as well as assist in the conduct of investigator -initiated research and division-specific research projects and operations. This position's ... in study team meetings, disease site group meetings, and ongoing protocol training/ compliance meetings. Supports in the monitoring of external sites and assists in… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …notifying research staff whose training has lapsed or is missing + Ensure compliance with investigator annual NCI registration requirements + Oversight of ODQ ... control of DF/HCC initiated clinical trial data, national protocol and investigator registrations, clinical trials education, and committee management. The Clinical… more