- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 10, 2025 Requisition # 106623 The Clinical ... Research Coordinator Associate is responsible for the overall management and implementation...assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the… more
- Wells Fargo (Lakewood, WA)
- **About this role:** Wells Fargo is seeking an Associate Bank Financial Advisor (LO) in Wealth and Investment Management as part of Wells Fargo Advisors. Learn more ... as part of the evaluation. Successful candidates must also meet ongoing regulatory requirements including additional screening, if necessary + US only: Obtaining… more
- Wells Fargo (Atlanta, GA)
- **About this role:** Wells Fargo is seeking a Registered Client Associate in Wealth and Investment Management as part of Wells Fargo Advisors. Learn more about the ... marketing campaigns, establishing and maintaining files to meet the firm's regulatory requirements, and establishing and maintaining filing and record keeping… more
- Wells Fargo (Bloomington, MN)
- **About this role:** Wells Fargo is seeking a Registered Client Associate in Wealth and Investment Management as part of Wells Fargo Advisors. Learn more about our ... marketing campaigns, establishing and maintaining files to meet the firm's regulatory requirements, and establishing and maintaining filing and record keeping… more
- UPMC (Pittsburgh, PA)
- …QA Associate will coordinate the quality management, safety, and regulatory activities for the Cellular Processing Facility and Adult and Pediatric Hematopoietic ... UPMC Hillman Cancer Center is hiring a full-time QA Associate , Cellular Therapy to support quality assurance for our...the liaison between nursing, the quality departments, and the regulatory departments of the hospitals to deliver safe and… more
- Parsons Corporation (San Antonio, TX)
- …collection of supporting documentation, coordinating clinical research studies, and maintaining regulatory requirements. In addition, the Research Associate III ... got what you're looking for. **Job Description:** Parsons is seeking a **Research Associate III** to support Naval Medical Research Unit - San Antonio (NAMRU-SA) and… more
- Cambrex High Point (Charles City, IA)
- …a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
- Charles River Laboratories (Ashland, OH)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... management, interpretation, and reporting of study data, and assuring the regulatory compliance of these projects. ESSENTIAL DUTIES AND RESPONSIBILITIES: *… more
- System One (Florham Park, NJ)
- …Sr. Associate /Manager, Medical Information (contractor) also requires proficiency with drug information databases and systems, as well as an understanding of ... Job Title: Senior Associate /Manager, Medical Information - Contractor Location: Florham Park,...and compliance guidelines and ensures knowledge of legal and regulatory requirements to appropriately respond to medical inquires, disseminate… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director, Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures scientific ... expertise necessary to design and deliver on clinical studies and programs. As an Associate Director, a typical day may include the following: + May function as… more