- Daiichi Sankyo, Inc. (Bernards, NJ)
- …validation of IT services and determining audit targets for GxP systems .ResponsibilitiesLeadership and Strategic DirectionThe Sr. Director, Data Quality and ... best approach for clinical development systems , PV systems and MA systems including data...stakeholders (RD, PV and MA) to drive timelines and report on key deliverables related to quality and compliance.… more
- Genmab (NJ)
- …and feel like a fit? Then we would love to have you join us!The RoleAs Senior Clinical Trial Associate (Sr CTA) you play a key role in supporting Clinical Trial Team ... expected to become Subject Matter Experts (SMEs) for assigned processes and systems .The primary location for this role is Utrecht, The Netherlands. Candidates… more
- Merck & Co. (Rahway, NJ)
- …analyzing system and passive data governance reports to ensure high quality data and timely and complete synchronization between systems . Acts to resolve all ... are not limited to, the following: Strong knowledge of Systems Applications and Products in Data Processing,...packages. Strong understanding of Enterprise Process Management to troubleshoot report /input templates (in cases of master data … more
- Eisai, Inc (MD)
- …want to hear from you. Job Summary The Medical Science Liaison (MSL) / Senior Medical Science Liaison (Sr. MSL) is a field-facing representative of US Medical ... with a primary responsibility of engaging in the exchange of scientific data and other medical and/or scientific information with external customers (healthcare… more
- Merck & Co. (North Wales, PA)
- …Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise ... the entire product lifecycle. - Primary Activities : Effective analysis and report programming development and validation utilizing global and TA standards and… more
- Merck & Co. (North Wales, PA)
- …deliverable quality.Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; and systems and database ... entire product lifecycle for assigned projects. Perform effective analysis and report programming development and validation utilizing global and Therapeutic Area… more
- Merck & Co. (Rahway, NJ)
- …partners, designs studies, authors study protocols, develops measurement questionnaires, case report forms, data analysis plans, final study reports, scientific ... Job DescriptionRole SummaryUnder the guidance of a senior leader, a Senior Principal Scientist/ Senior Director, has primary responsibility for developing… more
- Merck & Co. (Rahway, NJ)
- …and/or develops mitigation strategies for review with clinical partners and senior leaders.--Responsible and accountable for utilizing key technological tools in the ... SAP system to ensure a robust and consolidated forecast for CFGs is maintained. Report clinical supply chain incidents to support the gathering of metrics in GCS to… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Primary responsibilities include validation protocol execution (IQ, OQ, PQ & PV), data analysis and final report preparation for utilities, equipment and ... in the pharmaceutical or biotechnology industry Experience preparing protocols, executing data analysis, and report writing Experience preparing protocols,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for patients and healthcare providers. We are a group of innovative, data driven, cross-functional leaders that focusing on driving the strategy and execution ... consumers are at the forefront of our strategies.RelationshipsReports directly to the Senior Vice President of Marketing & Patient Solutions. This role collaborates… more
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