- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is ... responsible for the effective management of GCP , GVP and GLP inspections. The GDQIM IML will...guidelines including the management of significant/complex quality issues and compliance activities. * Extensive experience with participating in, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Takeda Pharmaceuticals (Boston, MA)
- …on quality compliance activities. + Provide guidance and support to GCP , PV Health Authority inspections including logistics. + Present insights to the health ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- IQVIA (Durham, NC)
- **Job Level: Associate / Director of Biostatistics,** **Early Phase Pharmacodynamics** **Location:** **Home-based in the US or Canada** **(East Coast Preferred)** ... **Job Overview:** As an ( Associate ) Director , you will liaise with cross-functional...resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Bristol Myers Squibb (Princeton, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , RBQM - HOCT, ICN will mainly be responsible for ... vendors, demonstrating effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and… more
- OneMain Financial (Irving, TX)
- …actionable insights into digital behaviors and performance. We are seeking an experienced Associate Director of Data Products to lead our shared data products ... and maintain best practices for data governance, data quality, and compliance with financial services regulations. **Stakeholder Management** : Engage with senior… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …for staff recruitment, development, coaching, mentoring, and performance management. **As an Associate Director , CDM Lead, a typical day might include:** + ... conduct of clinical research studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOPs) within assigned… more
- Bristol Myers Squibb (San Diego, CA)
- …This position will be based in San Diego, CA or Lawrenceville, NJ. **Summary:** The Associate Director , Clinical Data Management, will play a crucial role in our ... as needed. + Contribute to SOP development and updates to meet regulatory compliance and operational needs. + 10% of travel required. **Basic Qualifications:** +… more
- ThermoFisher Scientific (Cambridge, MA)
- …is vital to helping our customers deliver life-changing therapies. **Position:** Associate Director /Senior Project Manager, Drug Development, FSP **Location:** ... and Issue Resolution at project level (RBQM/RESOLVE). + Ensures project team compliance with organization policies, SOPs, ICH- GCP , regulatory and project… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Laboratory Data Management is accountable for the ... oversight for Data Management resources, CROs, and vendors to ensure compliance with the program standards, Policies, SOPs, external/internal standards, Good… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …systems, with a strong focus on ensuring inspection readiness and regulatory compliance . **_DIMENSIONS AND ASPECTS_** + As VBU representative for the study ... for clinical trial documentation and its lifecycle management ensuring compliance with the evolving regulatory requirements, industry trends, technological… more
- e CancerCare (Fresno, CA)
- Purpose: The Director , Clinical Trials & Research, for CCARE Physicians, PC, is responsible and accountable for the daily operations and management of staff, of the ... the finance department, the overall financial activities of the department. Assures compliance with all regulatory requirements and standards of good practice (… more
- RWJBarnabas Health (Long Branch, NJ)
- Assistant Director , Institutional Review Board - Long Branch, NJReq #:0000197806 Category:Laboratory and Medical Technologist Status:Full-Time Shift:Day ... 300 Second Avenue, Long Branch, NJ 07740 Job Title: Assistant Director Location: Monmouth Medical Center Department: Institutional Review Board Req#: 0000197806… more
- Ensono (Downers Grove, IL)
- Director of Project Management GovernanceDowners Grove, ILJR011899 At Ensono, our **Purpose is to be a relentless ally, disrupting the status quo and unleashing our ... and Passion. **Job Summary:** We are seeking a highly skilled and experienced Director of Project Management Governance Leader to join our team. This individual will… more
- US Foods (Rosemont, IL)
- …(https://www.myworkday.com/usfoods/d/task/2998$47185.htmld) Join Our Community of Food People! The Director , Digital Marketing Engineering, will lead our Marketing ... + Implement best practices for data governance, quality, and compliance across marketing systems. + Leverage CDP and AI-driven...**Remote** : This role is fully remote, and the associate is expected to perform assigned responsibilities from a… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …through early and/or late phase development. The Senior Manager reports to the Associate Director , Clinical Sciences and collaborates closely with Medical ... of regulatory documents; may perform quality review + Maintains compliance in accordance with FDA, EMEA, ICH and ...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- AbbVie (North Chicago, IL)
- …where staff and studies/programs will succeed + Execute clinical programs in compliance with quality standards (ICH/ GCP , Global Regulations, and AbbVie policies ... Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and operations to bring… more
- University of Colorado (Aurora, CO)
- …part- or full-time (0.5 - 1.0 FTE). This position reports to the LEAD Center Associate Director for Research. **Work Location:** **Why Join Us:** **Why work for ... perform phlebotomy and intravenous catheter placement to collect blood in compliance with university policies and procedures. + Assist with developing… more
- Amgen (Washington, DC)
- …Suppliers for Amgen sponsored clinical trials + Monitoring and evaluating Supplier compliance and data quality + Tracking corrective actions in relation to ... external partners, including study teams, functional leads, procurement, quality, compliance , and suppliers + Support business functions with evaluation, selection,… more
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