- Santander US (Coconut Grove, FL)
- Senior Associate , Cyber and Digital Risk Management Country: United States of America **Your Journey Starts Here:** Santander is a global leader and innovator in the ... Talk to You!** **The Difference You Make:** The Sr. Associate , Cyber & Digital Risk monitors activities to minimize...that the oversight is adequate to minimize compliance and regulatory risk by resolving issues and ensuring adherence to… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …excellence of our academic community. **Description** Reporting directly to the Senior Associate Dean for Faculty Affairs, the Associate Dean, Faculty Affairs ... Administration, provides leadership, management and oversight for business, legal and regulatory matters involving the School of Medicine faculty. The Associate … more
- Sanofi Group (Framingham, MA)
- …clinical, manufacturing, commercial, and other internal business partners to enable successful regulatory outcomes + Prepare, review and approve design control ... **Job Title:** GRA Device Lead ( Associate Director) **Location** : Morristown, NJ/ Cambridge, MA/...critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- **Overview** The Quality Assurance Associate - Supplier Management is responsible for the execution of day-to-day quality activities related to the company-wide ... a focus on supplier management ensuring that manufactured products meet quality, regulatory , and compliance standards before release. This role involves meticulous … more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …oversight and risk-based data management strategies, standards and processes. The Associate Director, Data Management will bring deep knowledge of industry best ... practices, regulatory requirements, and systems and processes that support efficient...including database build, cleaning, reconciliation, and locking activities across multiple clinical trials to ensure timely, accurate, and complete… more
- Organon & Co. (Jersey City, NJ)
- …in the non-clinical field in meetings with internal/external stakeholders + Author and review of non-clinical CTD modules for regulatory submission (eg, IND, ... impurity-related regulatory guidelines and GxP requirements. + Experience with review and authoring non-clinical sections of regulatory dossiers (eg, NDAs)… more
- Takeda Pharmaceuticals (Lexington, MA)
- …true to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device ... deliver device clinical outcomes that exceed quality benchmarks and regulatory standards. **Core Responsibilities:** **Device Clinical Strategy & Risk Management:**… more
- Penn Medicine (Philadelphia, PA)
- …involvement (research initiatives, resident program), special clinical programs, multiple clinical specialties, complex regulatory requirements, management ... **Hours: Full-Time** Summary: + In collaboration with leadership, the Associate Practice Manager provides strategic operational leadership, supervision and direction… more
- Stanford University (Stanford, CA)
- …for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board… more
- JPMorgan Chase (Brooklyn, NY)
- …the Firm's capital adequacy. As a CCAR Y-14 Reporting & Analysis - Senior Associate within the Firmwide Regulatory Reporting & Analysis team, you will be ... FR Y-14A reporting **Job responsibilities:** + Support and coordinate multiple aspects of FR Y 14A reporting process, and... reporting control and governance framework + Oversee the review and maintenance of the regulatory reporting… more