- Geisinger (Wilkes-Barre, PA)
- …work experience is required. Prior Oncology and/or research experience is strongly preferred . Job Duties: + Coordinates and implements clinical research studies. + ... study protocols. + Administers and monitors study drug as directed by the investigator and clinician. + Performs triage nursing assessments of subjects as needed. +… 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
- Cedars-Sinai (Beverly Hills, CA)
- …activity, research manuscript publications, program progress narratives, scientific highlights, investigator 's, other support, young investigator awards, Core ... of regulatory/IRB operations from start-up to closeout. + Serves as sub/co- investigator on clinical trials, observational research, and biobanking protocols. +… more
- ProMedica Health System (Toledo, OH)
- …Summary:** As the Clinical Research Scientist, you implement investigator -initiated clinical research studies through collaboration with physicians, researchers, ... Able to independently prepare and implement research protocols as principal investigator . + Prepares draft manuscripts from study data. Performs independent… 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
- Actalent (Lima, OH)
- …events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor. + Prescreen study candidates. + Obtain informed consent per ... ECGs, and other test results for completeness and alert values, ensuring investigator review in a timely fashion. + Discuss study medication, required procedures,… more
- Tufts Medicine (Boston, MA)
- **General Summary:** This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. Our Tufts ... to job area. **Job Overview** This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. **Job… more
- University of Michigan (Ann Arbor, MI)
- …as a Research Area Specialist Intermediate who will work alongside the Principal Investigator in the Department of Family Medicine and a team of investigators across ... study-related activities and help oversee project staff and milestones. The Principal Investigator and supervisor for this position in Dr. Kimberly McKee, an… more
- Astellas Pharma (Northbrook, IL)
- …planned clinical trials on assigned development programs (eg, develop protocols, investigator brochures, CRFs, informed consents, and clinical study reports and ... analysis for DMC/DSMB/DEC forums or regulatory submissions. + Provides training at investigator meetings and site initiation visits with clinical trial staff, and… more