- Guidehouse (Richardson, TX)
- **Job Family** **:** Investigator **Travel Required** **:** None **Clearance Required** **:** None **What You Will Do** **:** + Perform reviews and investigations of ... guidelines (eg, BSA, OFAC, FinCEN guidance). + Knowledge of Financial Crimes Compliance functions such as OFAC Sanctions, Anti-Money Laundering, KYC, CDD, EDD and/or… more
- Dartmouth Health (Lebanon, NH)
- …research and a full range of clinical research duties including regulatory compliance . * May arrange/schedule required tests and other appointments. * Independently ... of the study operations (subject management/regulatory) with minimal oversight from the investigator or their designee. * Oversees subject management, such as data… more
- Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
- …and meet Department of Defense (DoD) and Defense Health Agency (DHA) standards for ethics and compliance . + Assist with the amendment of existing investigator ... In consultation with the PI's and the CIDH, prepare new investigator -initiated trials, coordinate the submission, and ensure final product development (presentation… more
- J&J Family of Companies (Titusville, NJ)
- …in ensuring that investigator grants comply with overall study costs and compliance guidelines. + Comply with requests from QA and auditors. + Work proactively ... team in the pricing, planning, execution and control of site/ investigator budgets and contracts. **You will be responsible to:**...may be performed as assigned. + Adhere to SOPs, ethics and departmental compliance as determined by… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …ADDITIONAL JOB DETAILS: + Provide administrative and research support to the Principal Investigator and Program Director for the execution of NIH funded project. + ... settings. + Work directly with international team staff to ensure compliance with project protocols and national/international research regulations, developing and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …other Harvard Medical School-affiliated hospitals. Administrative: + Assists principal investigator with protocol development. + Assists principal investigator ... appropriate with the Institute's protocol review process. + Assists the principal investigator in developing the protocol budget. + Collaborates with the Dana-Farber… more
- J&J Family of Companies (Irvine, CA)
- …R&D Department to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for JNJ MedTech Neurovascular . ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); . Ensures applicable trial registration (eg on… more
- J&J Family of Companies (Irvine, CA)
- …to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones; + Oversees/executes feasibility, selection, ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports, ); + Supports applicable trial registration (eg… more
- Dartmouth Health (Lebanon, NH)
- …has no supervisory responsibilities and works under direct supervision of the Principal Investigator or designee. They cannot perform any tasks that by state or ... study operations (subject management/regulatory) with substantial oversight from the investigator or their designee. * Primarily supports subject management, such… more
- Sumitomo Pharma (Topeka, KS)
- …+ Assesses and communicates regulatory requirements ensuring activities are in compliance with applicable regulations and guidelines + Leads documentation of ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed… more