- University of Colorado (Aurora, CO)
- … research regulatory standards and guidelines. + Manage all regulatory aspects of study start-up and ongoing maintenance, ensuring studies open on time and ... ** Research Services Professional (Regulatory and Pre-Award) - Open...compliant. + Maintain thorough and organized records for all studies to ensure compliance with FDA regulations, study… more
- ConvaTec (Lexington, MA)
- …Convatec's policies and SOPs. **Key Responsibilities:** + Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all ... of Clinical Research Organizations (CROs) and other vendors for clinical studies that are outsourced to third party vendors (with the exception of data… more
- ThermoFisher Scientific (Frederick, MD)
- …all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting. + Reviews and understands ... individual career goals while taking science a step beyond through research , development and delivery of life-changing therapies. With clinical trials conducted… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …centralized risk-based monitoring oversight activities as assigned. * May support the Study Manager to formulate regional monitoring strategy, forecasting of ... **Overview** The Sr CRA will be responsible for monitoring clinical studies at the site level ensuring adherence to protocols, timelines, ICH/GCP guidelines, and… more
- AdventHealth (Orlando, FL)
- …Programs (OSP). Prepares and/or reviews all required documentation for clinical research study start up, execution, modification, renewal, and termination ... and perform the nursing care of participants and collect data for assigned research projects. The CRC II follows study specific protocol guidelines, communicates… more
- AbbVie (Irvine, CA)
- …I in the Tissue Materials Science group is responsible for directing research and/or project activities and professional development of a group of scientists ... personnel. He/She/They independently conceive, execute and communicate novel multi-disciplinary research or development strategies that achieve project for the… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: This role will act as the project manager for a large multi-site clinical trial where the clinical site is also the coordination center for the clinical ... clinical trial at the Sponsor Level including but not limited to: procuring study drug, site selection and management, vendor selection, consent form development, … more
- ThermoFisher Scientific (Greenville, NC)
- …study documents in support of the regulatory filing + Responsible for overseeing study financial reconciliation + Ensure studies are "inspection ready" at all ... **Experience: 6+ years' experience in pharmaceutical industry and/or clinical research organization, including 4+ years clinical study management/oversight,… more
- Alaka'ina Foundation Family of Companies (San Antonio, TX)
- …Ability to develop and coordinate the implementation of clinical research studies , including regulatory requirements, maintenance of study records and all ... Research Associate III Location TX - San Antonio...space. + Ability to develop, organize and maintain the study database and data validation. + Maintains data and… more
- Gilead Sciences, Inc. (CA)
- …+ Manage **day-to-day administration and operations** for ISRs, collaborative and non-interventional studies from concept approval to study closure: + Lead ... Kite and help create more tomorrows. **Job Description** Kite's External Research Program (ERP) advances our enterprise portfolio through external innovation and… more