- Gilead Sciences, Inc. (Foster City, CA)
- …documents including safety reports, amendments, supplements and license renewals to clinical trial applications and marketing authorizations original INDs/CTAs ... communicate changes in regulatory information to project teams and senior management in a timely manner. + Initiates local...Work is performed with no immediate direction from a senior Regulatory Affairs professional. + Is recognized as a… more
- Veterans Affairs, Veterans Health Administration (White River Junction, VT)
- …center performance measures; monitor, verify, correct, and upload all transcription/medical speech recognition to maintain completeness and accuracy of health ... Duties include but are not limited to: Responsible for abstraction of clinical information for ongoing regulatory reviews. Contacts physicians and other ancillary… more
- University of Maryland, Baltimore (Baltimore, MD)
- …scientist or physician-scientist with expertise in real world data and novel clinical trial design/execution with particular emphasis on oncology sciences to ... in clinical research with allied expertise in real world evidence, novel clinical trial design (such as adaptive and pragmatic studies), and a deep… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... Support daily operations to ensure seamless interaction of core applications by being a senior member of the Materials Flow team. + Own the knowledge management and… more
- AbbVie (Mettawa, IL)
- …collaborate with CI to align on recent developments with competitor earnings reports, clinical trial data, filing, and approval timelines. + Global Commercial ... and have a team of three, comprised of two Associate Directors and a Sr . Analyst. This...Development I cooperation to understand internal clinical trial timelines and probabilities for success… more
- Boehringer Ingelheim (Ridgefield, CT)
- …under their responsibility as delegated by TA HoEM. + Review and approve final Clinical Trial Reports, Clinical Trial Protocols, scientific publications ... + Ensures the review of the Master Plans, related Clinical Development plans and Clinical Trial...years (combination of hospital, academic and industry experience),inclusive of senior leadership role/s; Clinical / pharma experience… more
- Boehringer Ingelheim (Ridgefield, CT)
- …as delegated by the Head of ExpMED of Inflammation. * Review and approve final Clinical Trial Reports, Clinical Trial Protocols, scientific publications ... * Ensures the review of the Master Plans, related Clinical Development plans and Clinical Trial...(combination of hospital, academic and industry experience), inclusive of senior leadership role/s; Clinical / pharma experience… more
- HCA Healthcare (Salem, VA)
- …will oversee the implementation and adherence to established treatment protocols and clinical trial protocols, ensuring regulatory compliance of the Primary ... assistance (tuition, student loan, certification support, dependent scholarships) + Colleague recognition program + Time Away From Work Program (paid time off,… more
- Mount Sinai Health System (New York, NY)
- …leaders, hospital and system leaders, and with external parties. **Grant and Clinical Trial Management** + Responsible for research enterprise including grants ... Integration and Administration of the Department of Medicine, other senior leadership of the Department, and MSM/W Hospital leadership...research compliance, and oversight of core facilities + Oversee clinical research and clinical trial … more
- University of Rochester (Rochester, NY)
- …of the URCC NCORP Research Base (an NCI funded $30+ million nationwide cancer clinical trial network with more than 35 partner institutions across the country), ... and Director of the URMC PEAK Human Performance Clinical Science Program, and Director of the Wilmot RENEW...University-wide Search Committees for Wilmot Population Science junior and senior faculty recruits (eg, new Wilmot Associate … more