- 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
- Dana-Farber Cancer Institute (Boston, MA)
- …(RC)** works under the direction of the Breast Oncology Principal Investigator (s), Regulatory Operations Manager, Clinical Research Manager and / or directly ... of assigned study monitoring and auditing visits with study coordinator, Investigator , DF/HCC QACT, Industry Sponsors, and third party auditors. **Clinical Trial… more
- J&J Family of Companies (Danvers, MA)
- …and parlaying clinical trial experience, knowledge, and feedback ("Voice of Investigator ") to Abiomed cross-functional partners such as R&D, medical affairs, ... open communication and relationships with key site personnel including the Principal Investigator , Research Coordinator, as well as regulatory and legal personnel. +… more