Project Manager, Study Operations, Cronos
4 semanas atrás
OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers. Responsibilities Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies. May be responsible for delivery and management of smaller, less complex, regional studies. Develop integrated study management plans with the core project team. Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures. Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance. Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally. Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts. Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans. May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary. Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles. Ensure the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward. Identify changes in scope and manage change control process as necessary. Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements. Adopt corporate initiatives and changes and serve as a change advocate when necessary. Provide input to line managers of their project team members’ performance relative to project tasks. Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Qualifications Bachelor's Degree Life sciences or related field (Required). 7+ years of prior clinical research experience including around 5 years project management experience in a global, client-facing environment. Strong written and verbal communication skills including a good command of English. Strong presentation skills. Strong problem solving skills. Ability to coordinate across functions to deliver results to quality and timeline metrics; experience partnering cross-functionally and with customers. Ability to make decisions and bring clarity to disparate information to inform actions and drive results. Employment type Full-time Seniority level Not Applicable IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA values diversity, inclusion, and belonging and is committed to empowering our mission to accelerate innovation for a healthier world. #J-18808-Ljbffr
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Project Manager, Study Operations, Cronos
3 semanas atrás
São Paulo, Brasil IQVIA LLC Tempo inteiro**Job Overview**Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...
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Sr Project Management Analyst, Study Operations, Cronos
3 semanas atrás
São Paulo, Brasil IQVIA Argentina Tempo inteiroProvide project related support and assistance for assigned project(s) and project teams with minimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical practices...
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Sr Project Management Analyst, Study Operations, Cronos
4 semanas atrás
São Paulo, Brasil IQVIA Tempo inteiroOverview Provide project related support and assistance for assigned project(s) and project teams with minimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical...
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São Paulo, Brasil IQVIA Tempo inteiroProvide project related support and assistance for assigned project(s) and project teams with mínimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical practices...
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Sr Project Management Analyst, Study Operations, Cronos
4 semanas atrás
São Paulo, Brasil IQVIA LLC Tempo inteiroProvide project related support and assistance for assigned project(s) and project teams with minimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical practices...
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Regional Clinical Study Manager
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São Paulo, Brasil BeiGene Tempo inteiroPLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Portuguese and English required. Spanish preferred. Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology General Description: - Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget -...
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Sr Project Management Analyst, Study Operations, Cronos
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São Paulo, São Paulo, Brasil IQVIA Tempo inteiro R$90.000 - R$120.000 por anoProvide project related support and assistance for assigned project(s) and project teams with minimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical practices...
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Assoc Project Management Analyst, Study Operations, Cronos
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Greater São Paulo Area, Brasil IQVIA Tempo inteiro R$60.000 - R$120.000 por anoProvide project related support and assistance for assigned project(s) and project teams with minimal supervision. Projects are typically larger in scope and complexity than those supported by staff at a lower grade. Will ensure all work is conducted in accordance with standard operating procedure (SOPs), policies and practices, good clinical practices...
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Regional Clinical Study Manager
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São Paulo, São Paulo, Brasil BeOne Medicines Tempo inteiro R$90.000 - R$120.000 por anoBeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.PLEASE SUBMIT ALL RESUMES/CV'S INENGLISHFOR...