- BeOne Medicines (Emeryville, CA)
- …site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ... ICH-GCP guidelines, local regulations, and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study… more
- ThermoFisher Scientific (Chicago, IL)
- …weather conditions **Job Description** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits ... to assess protocol and regulatory compliance and manages required documentation. Manages procedures and...business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to… more
- SUNY Upstate Medical University (Syracuse, NY)
- …and experience. Preferred Qualifications: Two years of experience in a cardiology clinical research . Work Days: M-F Daytime Hours Message to Applicants: ... primary function of this position is to assist the investigators in their research studies within the Cardiology Division of the Department of Medicine. This… more
- Reckitt (Parsippany, NJ)
- Regulatory and Safety Affairs Associate City: Parsippany **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our ... of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working...grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate , Regulatory… more
- ThermoFisher Scientific (Austin, TX)
- …approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May ... client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance… more
- ThermoFisher Scientific (Chicago, IL)
- …approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May ... client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance… more
- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret ... regulatory intelligence specialists have continued access to regulatory , clinical trial, and public domain information...practices. + Review overall quality of ad hoc query research for requested regulatory topics and confirm… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …our day and improving the lives of patients for generations to come. As an Associate Director, Global Regulatory Affairs, you will act as the Regional ... or projects to lead, manage and oversee simultaneously. You will define the regulatory strategy, plans and objectives for assigned products or projects. You may act… more
- Rush University Medical Center (Chicago, IL)
- …strongly preferred (Certified Clinical Research Professionals (CCRP), * Certified Clinical Research Associate (CCRA), * Certified Clinical ... with sponsors and regulatory partners, and ensuring standardization and quality across clinical research processes. The Lead CRC may serve as an interim… more
- Rush University Medical Center (Chicago, IL)
- …strongly preferred (Certified Clinical Research Professionals (CCRP), * Certified Clinical Research Associate (CCRA), * Certified Clinical ... or training. **Preferred Job Qualifications:** **Experience:** * 2-5 years' experience in clinical research conduct, regulatory management, or research… more