- City of New York (New York, NY)
- …requests for Agency records and witness appearances in the defense of approximately 3 ,000 personal injury cases each year. The unit seeks a highly organized and ... to offices and courthouses in all 5 boroughs, approximately 3 times each week, to testify under oath at...under oath at Examinations Before Trial and at Trials. INVESTIGATOR - 31105 Qualifications 1. A four-year high school… more
- Bayer (Whippany, NJ)
- …in Radiology. This role encompasses clinical development phases from Phase 1 to Phase 3 , with an emphasis on late-phase development. You will focus on the purposeful ... documents or components of key documents (eg, Clinical Study Protocol, Investigator Brochure, Clinical Study Report, regulatory documents, etc.); + Develop and… more
- City of New York (New York, NY)
- Job Description APPLICANTS MUST BE PERMANENT IN THE ASSOCIATE FRAUD INVESTIGATOR CIVIL SERVICE TITLE. The DSS Accountability Office (DSS-AO) is responsible for ... commit fraudulent acts against HRA as per SSL 348.2; 348. 3 . Within BFI, the Investigation Division (ID) oversees and...Pearl Street, NY NY Hours/Schedule: 9AM -5PM ASSOCIATE FRAUD INVESTIGATOR ( - 31118 Qualifications 1. A four-year high… more
- Mayo Clinic (Rochester, MN)
- …members hold $31M in external research funding (annual direct costs), of which $20. 3 M is federal peer-reviewed funding (primarily from NIH and DOD) and $10.6M ... more than 7,300 physicians and scientific investigators, Mayo Clinic cared for more than 1. 3 million unique patients who came from all 50 US states and 135… more
- Bristol Myers Squibb (San Diego, CA)
- …regulatory authority interactions, design, and execution of Phase 0 to Phase 3 clinical trials, and medical monitoring. This role provides medical direction and ... of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial… more
- University of Michigan (Ann Arbor, MI)
- …Concepts and Research Design 2. Ethical Participant Safety Considerations 3 . Investigational Products Development and Regulation 4. Clinical Study Operations ... team to coordinate and execute aspects of sponsor and/or investigator initiated clinical studies. These activities include, but are...from SoCRA or ACRP prior to applying.) + Minimum 3 years of directly related experience in clinical research… more
- GE HealthCare (Boston, MA)
- …teams on legal issues related to GE HealthCare sponsored and investigator -initiated research and collaboration proposals and engagements. **Job Description** **Key ... leaders on legal and compliance issues surrounding company-sponsored and investigator -initiated research and collaboration proposals and engagements * Structure,… more
- Beth Israel Lahey Health (Burlington, MA)
- …and other colleagues related to Research conducted within the department. 3 ) Functions as an interdepartmental liaison, evaluating, coordinating, and facilitating ... occurrence of adverse events or toxicities in collaboration with the study investigator ; Ensures non-serious and serious adverse events are properly documented, and… more
- North Carolina Agriculture & Technical State Unive (Greensboro, NC)
- Description: The position provides support and reports to the Principal Investigator in all aspects of field assessment of micropropagated plants and overall ... as a resource person on behalf of the Principal Investigator , and are responsible for overall field operations (including...training and/or related experience. Advanced: 4 year degree + 3 years of directly related experience; or an equivalent… more
- Lilly (Indianapolis, IN)
- …+ Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports. + ... study-related questions. + Provide scientific input for site selection, investigator meetings, steering committees, and clinical trial training. + Participate… more