- Sanford Health (Sioux Falls, SD)
- …Looking For: * Active Registered Nurse * Prior research experience (strongly preferred ) * A collaborative, patient-centered mindset What We Offer: * Supportive and ... and compliant investigational treatment or intervention and follow-up. Attend investigator meetings and coordinate pre-study site visits. Monitor enrollment goals… more
- BeOne Medicines (Emeryville, CA)
- …concepts, synopses, protocols, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts ... and execution of clinical studies + Provide scientific expertise for selection of investigator and vendors + Train BeOne colleagues, CRO staff, and study site staff… more
- UTMB Health (Galveston, TX)
- …for preparation of Contributing Scientist Reports. + Works with Principal Investigator and/or Study Director on development of required biosafety approvals, animal ... + Complies, writes, and effectively communicates project results to the Principal Investigator and/or Study Director. + Manages all aspects of the lab, including… more
- United Therapeutics (Research Triangle Park, NC)
- …team and other stakeholders to provide biostatistical resources for investigator -sponsored clinical studies and address internal/external investigator queries ... expert input, conduct thorough reviews, and grant approval for submitted investigator -sponsored clinical studies, external investigator queries of UT databases,… 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 ... to work effectively and collaboratively in a complex academic environment. ** Preferred Job Qualifications:** * Bachelor's degree in Health Sciences or related… more
- BeOne Medicines (Emeryville, CA)
- …concepts, synopses, protocols, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts ... execution of clinical studies. + Provide scientific expertise for selection of investigator and vendors. + Provide scientific and medical support throughout conduct… more
- Gilead Sciences, Inc. (Foster City, CA)
- …input on activities including study protocol preparation, other study or investigator documentation, medical monitoring, data analysis plans, study reporting, and ... including but not limited to assessment of eligibility criteria, addressing investigator questions, safety monitoring, and ensuring high data quality through data… more
- Guthrie (Sayre, PA)
- …clinical research organization + Certifications in research administration (eg, SOCRA, ACRP) preferred . Leadership & Strategic Planning + At least 5 years of ... investigational drug and device clinical trials + Oversight of investigator -initiated research. Determine feasibility, scientific review, funding and resource… more
- University of Pennsylvania (Philadelphia, PA)
- …performed, reporting adverse events and ensuring review and appropriate follow-up by investigator , monitoring patient care and treatment side effects in concert with ... of a team as well as independently; (5) knowledge or experience in cancer preferred but not required; (6) ability to work flexible hours; (7) possess working… more
- University of Pennsylvania (Philadelphia, PA)
- …requirements, and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report ... contribute to study-related meetings, including but not limited to Investigator Meetings, Site Initiation Visits, Intermediate Monitoring Visits, Close-out Visits,… more