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... strategic approach for Global Regulatory Compliance Identify and monitor key performance ... areas of improvement and ensuring compliance with current regulatory policy, legislation ... Safety & Risk Management, Global..
... results. Profile Description The Associate Director Clinical Data Capabilities is an essential ... an essential role within the Clinical Trial Business Capabilities group that ... ownership and accountability for..
... of our portfolio while ensuring quality, compliance and ethics. This role requires ... the BMS strategy without compromising Quality, Compliance and Ethics. Drives Functional Service ... adhering to the..
... business results. As the Associate Director of clinical quality performance analysis, you develop and ... deliver data-driven insights on the quality of trial operations for BMS's ... innovative pipeline...
... Information Bristol Myers Squibb Associate Director - Global Quality Clinical Trials and Safety in Princeton ... of the job Conduct Good Clinical Practice (GCP) and pharmacovigilance (PV) ... as..
... design and geographic scope). Prepares clinical section of regulatory document. Collaborates ... Reviews and oversee completion of clinical trial protocols. Provides medical and/or ... medical and/or scientific direction to..
The Regeneron Associate Director, GVP Quality Management Lead (QML) is a ... key position that will drive quality in Global Development by providing ... leadership for all aspects of quality..
... ensure delivery of timely, high quality, and ethical medical publications in ... publication plans in accordance with clinical trial results and changes in ... Reviews publication drafts for scientific..
... Summary Reporting into the Sr. Director, Innovation, the Associate Director, Innovation is a member of ... Patient Safety (WWPS). The Associate Director, contributes to the ongoing development, ... Takes..
... support the development of high quality medical publications to ensure clear, ... to BMS medicines. The Associate Director, Medical Publications for Oncology Clinical Collaborations will be part of .....
... Capability projects ensuring efficiency, consistency, quality of work and compliance with external regulations and internal ... leads, business users, and Global Quality function to ensure CSV projects ... and..
... Position reports to the Executive Director of Worldwide Scientific Publications within ... Publications Leadership Team, the Senior Director of WW Hematology/Cell Therapy Scientific ... delivery of timely and high..
... defined as part of the Quality Management System Architecture. The BCP ... of process metrics to achieve quality outcomes . The GPO will ... the liaison between the Global..
... Information Bristol Myers Squibb Associate Director, Medical Safety Assessment Physician in ... certain postmarketing commitments, and ensuring compliance with global regulatory requirements. Position ... as safety sections of relevant..
... diseases and immune disorders.SummaryThe Senior Director, Site Contracts & Budget Management ... oversight to all studies in compliance with internal processes and external ... CRO partners and the Sr...
... make a difference. The Executive Director, Clinical Development & Quality Operations is a critical management ... management position within the R&D Quality organization that is responsible for ... oversight..
... individual and team success. nnnOur Quality department located in our Monmouth ... immediate need for an experienced Director, Quality Compliance. nnnThe Director, Quality Compliance provides quality compliance leadership and..
... results. Profile Description The Associate Director Clinical Trial Execution Capabilities is an ... an essential role within the Clinical Trial Business Capabilities group that ... ownership and accountability for..
... Continuous Improvement and Change Management Director is accountable for the development, ... support the enhancement of the clinical Quality Management System, and that is ... aligned with, all R&D..
Medical Director -Publication Planning Publications- Publication Planning ... activities Creation, execution and ensure compliance of scientifically sound publications & ... and relationship building Mentoring, directing, quality control/quality assurance of junior..
Job Information Humana Director, Care Delivery and EMR/EHR Technology ... Livingston New Jersey Description The Director, Technology Solutions devises an effective ... and the core EMR/EHR. The Director, Technology Solutions..
... philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory ... policy requirements. Ensure provision of quality patient care while maintaining cost-effective ... patient care while maintaining cost-effective..
... Research and Development (R&D), Global Clinical Operations (GCO), Global Data Management ... Centralized Monitoring is responsible for clinical trial data acquisition, quality review, and standards governance for ... Summary..
