- IQVIA (Carlsbad, CA)
- …of 1 year of on-site monitoring as well as experience monitoring in oncology ._** Job Overview Perform monitoring and site management work to ensure that sites ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… more
- Taiho Oncology (Pleasanton, CA)
- …development in academic and/or industry, including experience as a medical monitor and (sub) investigator in oncology clinical trials. + ≥ 3 years in ... oversight, and analysis of Phase 1-4 oncology clinical trials. This position will be the medical...documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report… more
- Taiho Oncology (Pleasanton, CA)
- …has responsibility assisting in design, execution and reporting of current and future clinical oncology trials ranging from phase 1 - 3. Additionally, this ... trials. Performance Objectives: + Collaborates with other key team members ( Medical monitor, Project Manager, Clinical Operations, Data Management,… more
- Bristol Myers Squibb (San Diego, CA)
- …RayzeBio aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility ... with a focus on GU cancers. This role provides medical direction and high quality scientific and clinical...clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review… more
- BeOne Medicines (San Mateo, CA)
- …having taken at least one study through from start to finish in a clinical development role. + Clinical oncology experience; candidates with exceptional ... The Director, Clinical Development will support BeOne Clinical and Medical assets by successful execution...synopses, protocols, and amendments o Informed consent documents; + Investigator Brochures o Clinical study reports; +… more
- BeOne Medicines (San Mateo, CA)
- The Executive Director, Clinical I/O Development will support BeOne Medicine's Clinical and Medical assets by successful execution of clinical ... synopses, protocols, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports +...study site staff on the therapeutic area, molecule, and/or clinical protocol + Provide scientific and medical … more
- Actalent (Sacramento, CA)
- …appointments such as EKGs or vitals. + Interact with nursing staff and medical assistants. + Collaborate with clinical staff to obtain insurance authorizations. ... to schedule appointments. + Maintain an enthusiastic attitude. Essential Skills + Clinical research experience. + Pre-screening patients. + Oncology knowledge. +… more
- Stanford University (Stanford, CA)
- …duties may also be assigned._ **DESIRED QUALIFICATIONS:** + Experience working with oncology clinical research studies. + Experience with Phase I-III ... Post Date 5 days ago Requisition # 106860 **Cancer Clinical Research Coordinator 2 - GI Oncology ...and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of medical terminology.… more
- Ascendis Pharma (Palo Alto, CA)
- …to study teams + Ensure successful completion of trial-related documents (including clinical trial protocols, investigator brochures, medical monitoring ... in the design, monitoring, data analysis, and interpretation of the Company's late-phase clinical trials in endocrinology. As such, the Medical Director is an… more
- Translational Research in Oncology (Los Angeles, CA)
- …you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is ... the place for you! Translational Research in Oncology (TRIO) is a global academic clinical ...would be a major asset + Good knowledge of medical terminology and clinical monitoring process +… more