- Mount Sinai Health System (New York, NY)
- …of hematology/oncology Principal Investigators and researchers with development of investigator -initiated clinical trial protocols. Must understand complex ... obtains approval from the Food and Drug Administration (FDA) for investigator -initiated clinical trials. Acts as primary contact for all FDA communication,… more
- Astellas Pharma (Northbrook, IL)
- … 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,… more
- Rush University Medical Center (Chicago, IL)
- …documents. * Maintains accurate records related to the regulatory aspects of clinical research. * May coordinate timely investigator assessment of safety ... case. **Summary:** This positions provides regulatory support for multiple clinical research studies, which may involve multi-centered cooperative group studies,… more
- Dartmouth Health (Lebanon, NH)
- …duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the ... Overview Clinical Research Coordinator II performs a full range...study operations (including subject management/regulatory) with oversight from the investigator or their designee. * Primarily supports subject management,… more
- Houston Methodist (Houston, TX)
- …care effectively and efficiently to research patients under the supervision of the Clinical Trials Manager and Principal Investigator . This position implements ... At Houston Methodist, the Clinical Research Nurse (CRN) position is licensed clinician...aspects and protocol requirements of research studies. Attends off-site investigator meetings. + Provides comprehensive nursing assessments to develop,… more
- IQVIA (Durham, NC)
- … submission documents, including clinical study reports, protocols, clinical overviews, investigator brochures, and summary documents; experience with ... abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug… more
- Bristol Myers Squibb (Princeton, NJ)
- …evidence generation book of work (including Medical Affairs Sponsored studies, clinical research collaborations, investigator -sponsored studies and select health ... of Cell Therapy MEG book of work (Medical Affairs sponsored studies, clinical research collaborations and investigator -sponsored studies) ensuring they are on… more
- UT Health San Antonio (San Antonio, TX)
- …School of Medicine at UT Health San Antonio (UTHSA) is recruiting a Clinical Investigator . This position will hold an appointment of Assistant Professor/Research ... as a researcher in hospital medicine. A portion of this position involves clinical work on housestaff and non-housestaff services at University Hospital as well as… more
- Houston Methodist (Houston, TX)
- …writing and editing abstracts, manuscripts, review articles, grant applications, clinical study protocols, investigator brochures, consent forms, presentations ... of both medical and technical science while working with scientific and clinical teams to concisely and clearly communicate technical medicine and science in… more
- Parexel (Oklahoma City, OK)
- …or Canadian equivalent + Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred ... across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical,… more