- Taiho Oncology (Princeton, NJ)
- …relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), ... and drug development, including experience as medical monitor and (sub) investigator on a clinical oncology trial. + At least...$375,000 annually. This pay range is based on the market range for positions of this type. However, base… more
- AbbVie (North Chicago, IL)
- …Product Surveillance, clinical study safety management, contribution to post market surveillance activities, input to compliant regulatory authority reporting, ... based on the clinical study requirements. + Responds to safety questions from investigator sites and IRBs regarding safety issues and queries. + Provides medical… more
- Taiho Oncology (Princeton, NJ)
- …documents such as study protocols and clinical study reports (CSRs), investigator brochures, DSUR, NDA/MAA registration documents and publications. + Reviews and ... ongoing and final clinical study data, protocols and CSRs, investigator brochures, DSUR, NDA/MAA registration documents and publications. +...$195K annually. This pay range is based on the market range for positions of this type. However, base… more
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); + Ensures applicable trial registration (eg on ... Associates (CRAs); + Oversees and supports the development and execution of Investigator agreements and trial payments. + Is responsible for clinical data review… more
- Parexel (Richmond, VA)
- …data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. ... visit reports in CTMS and provides timely feedback to the Principal Investigator , including follow-up letter, within required timelines and in line with Client… more
- Stanford University (Stanford, CA)
- …staff, Stanford offers career development programs, competitive pay that reflects market trends, and benefits that increase financial stability and promote healthy, ... define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study… more
- Stanford University (Stanford, CA)
- …more clinical studies. Work under close direction of the principal investigator and/or study coordinator/supervisor. At Stanford University School of Medicine, the ... staff, Stanford offers career development programs, competitive pay that reflects market trends, and benefits that increase financial stability and promote healthy,… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of complex, single or multi-center clinical trials, including Principal Investigator (PI)-initiated trials, NIH-funded (eg, UG3/UH3), and industry-sponsored studies ... trials. + Protocol and Consent Form Development: Collaborate with the Principal Investigator (PI) to develop protocols and consent forms for initial applications and… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …control of DF/HCC initiated clinical trial data, national protocol and investigator registrations, clinical trials education, and committee management. The Clinical ... staff whose training has lapsed or is missing + Ensure compliance with investigator annual NCI registration requirements + Oversight of ODQ staff who provide direct… more
- Parexel (Columbus, OH)
- …data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. ... visit reports in CTMS and provides timely feedback to the Principal Investigator , including follow-up letter, within required timelines and in line with Client… more