- AbbVie (Florham Park, NJ)
- …Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Process Compliance Associate is an ... the Quality Control, Compliance , and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP… more
- Taiho Oncology (Princeton, NJ)
- …Summary: The Study Associate II is accountable for the performance and compliance of an assigned protocol and sites. The incumbent supports Clinical ... the progress of CRO/vendor's activities. + Identifies and resolves clinical study conduct issues and ensures site compliance...or close out activities. If delegated these tasks, Study Associate III will be supported by the clinical… more
- Merck (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Clinical Trials Operations, Computer Science, Design, Detail-Oriented, Ethical Compliance , Ethical Standards, GLP Regulations, Good Clinical Practice (GCP),… more
- Penn Medicine (Cape May Court House, NJ)
- …employees shape our future each day. Are you living your life's work? Clinical Services Associate (Medical Assistant) **Entity:** ( Clinical Care Associates) ... that actively supports your career growth? If so, a Clinical Services Associate opportunity at Penn Medicine...+ Orders supplies for the office and generates front-end process reports as requested. Other / Regulatory: + Ensures… more
- Penn Medicine (Somers Point, NJ)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... Medicine Somers Point- 155 Brighton Ave** **Hours: Full-Time** **Job Summary:** The Clinical Services Associates (CSA) assists the practice manager and physicians in… more
- Merck (Rahway, NJ)
- …development process & connectivity between functions supporting pipeline (ie clinical development, CMC, supply chain, & human health), and balancing needs of ... Leadership, Data Analysis, Drug Development, Logistics, Multiple Therapeutic Areas, Process Optimization, Publications Management, Regulatory Compliance , Risk… more
- Organon & Co. (Jersey City, NJ)
- …relevant regulatory documents of assets in Organon portfolio. + Ensure that non- clinical studies are conducted in compliance with relevant regulations, ... **Job Description** **The** **Position** The Non- Clinical Safety Assessment Representative within the Non- Clinical...manage multiple projects and shifting priorities. + Ability to process and articulate complex ideas in a manner that… more
- Regeneron Pharmaceuticals (Warren, NJ)
- As an Associate Director, Global Procurement, you will be accountable for defining and supporting the implementation of our Companion Diagnostics and Clinical ... success, efficiency, growth, and results. * Manages category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable. *… more
- Regeneron Pharmaceuticals (Warren, NJ)
- The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron's procedures ... and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in … more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their...planning: Set up the annual strategy to action (S2A) process of making sure the departmental strategy is aligned… more
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