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Team matrix interactions of the SRP include project management, finance, legal, quality assurance & compliance, clinical supplies, regulatory affairs, data management, medical writing, biostatistics, global safety, global medical affairs, clinical operations, and other scientific and business-related disciplines.
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The Director, SPML will be a key partner to the Global Regulatory Leader (GRL), Compound Development Team Leader (CDTL) and Project Management Leader (PML) in driving the timely delivery of major NDA/BLA/MAA submissions.
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This person will work closely with the clinical project scientist team and Clinical Leader in Late Development, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless and integrated execution of study start-up planning, oversight, and reporting of clinical studies in Oncology.
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A minimum of three (3) years of progressive experience executing in sales, CPG marketing, supply chain and/or project management; experience with HCP a strong plus. We are looking for a talent to join the North America Professional Marketing Team based in Summit/Skillman NJ, USA, as HCP Marketing Specialist as part of the HCP Professional Capabilities & Operation Team. The HCP Marketing Specialist will help drive consistency and efficiency across our professional marketing teams, work directly with our sales force leaders, IT and vendors to optimize activations, and leverage project management skills to help the teams execute with excellence.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Advanced proficiency with MS Excel is required; MS PowerPoint, Project Management software, and experience with one or more of the following platforms: Salesforce, Tableau, Alteryx, Python, SQL, highly preferred.
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Successful execution of product life cycle strategy for an assigned portfolio of products with a mid/high level of complexity, including Improve the competitiveness of the assigned products through alignment with P&L targets and active project portfolio management under guidance from Life Cycle Management; liaise with R&D for life cycle and design change projects for legacy product lines.
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Project Management - Team Lead or Team Member for Contract ing projects and/ or community events. The Global Services Contracti ng Co-Op is a 20-week program that encompasses functional & professional development, as well as completion of project(s) related to strategic business initiatives.
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Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders.
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Contribute to the development and delivery of appropriate Global EGS (Evidence Generation Strategies) and EDS (Evidence Dissemination Strategies) to support New Product Development and Life-Cycle Management, with collaborative relationships with all relevant Clinical, R&D and Regulatory partners ensuring cross-functional alignment.
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The MedTech Surgery Senior Regulatory Program Lead will be a responsible member of a Regulatory Affairs Team dedicated to developing and evaluating regulatory strategy in partnership with the assigned regulatory and clinical project leads.
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Experiences in crisis management, change management, and project management. Accountable for site qualification and validation programs for facility, equipment utilizing Quality Risk Management tools and associated documents.
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Oversee project assignment, workload distribution and problem resolution with direct reports and, as needed, team management and other functions. Have knowledge of GCO Standard Operating Procedures (SOPs) and fulfill the responsibilities per those SOPs. Ensure adequate, timely and compliant monitoring and management of clinical studies conducted in their TA.Ensure that team meets project deliverables according to timelines, within budget, and with quality.
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Johnson & Johnson is recruiting for a Clinical Project Scientist, Oncology. May partner with the lead CPS/Cross Functional Trial Team to mitigate issues in initiation of clinical trials and may participate in review of Monitoring Guidelines, SET/IDMC Charter, Statistical Analysis Plan, Data Management, and Safety Management Plans.
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The Manager, Global Clinical Operations (GCO) will be responsible for the direct functional management of a group Site Managers (SMs) in the Oncology Therapeutic Areas (TA) within GCO U.S. at Janssen.
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Job Field: Clinical Trial Project ManagementOrganization: Janssen Research & Development, LLC (6084) Learn more at Key Responsibilities:Performance and development in accordance with Performance Management guidelines, including coaching, mentoring and routine feedback.
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project management jobs Company: Johnson Johnson
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