Regulatory and Start Up Manager - Medical Devices - Home- based in SpainJoin to apply for the Regulatory and Start Up Manager - Medical Devices - Home- based in Spain role at PharmiWeb.Jobs :
Global Life Science JobsRegulatory and Start Up Manager - Medical Devices - Home- based in Spain3 days ago Be among the first 25 applicantsJoin to apply for the Regulatory and Start Up Manager - Medical Devices - Home- based in Spain role at PharmiWeb.Jobs :
Global Life Science JobsGet AI-powered advice on this job and more exclusive features.Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.Internal Job DescriptionJob OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.Home Based role requiring experience with medical devices submissions (MD / IVD) as well as Site Activation Oversight and Spanish language fluency.Essential FunctionsOversee the execution of Site Activation (including pre-award / bid defense activities) and / or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines.Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required.Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan.Create and / or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required.Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team.Determine regulatory strategy / expectations and parameters for submissions and all necessary authorizations, identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan.Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.Execute operational strategy / expectations for maintenance of clinical study approvals, authorizations and review / negotiation of contracts and essential documents.Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information.May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations / training to clients, colleagues and professional bodies, as required.May be involved in activities related to monthly study budget planning and reviews.QualificationsBachelor's Degree Life sciences7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role.Thorough understanding of regulated clinical trial environment and in-depth knowledge of drug development processDemonstrated proficiency in using systems and technology to achieve work objectivesGood regulatory and / or technical writing skillsStrong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelinesIQVIA 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, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.Seniority levelSeniority level Mid-Senior levelEmployment typeEmployment type Full-timeJob functionJob function Health Care ProviderIndustries Staffing and RecruitingReferrals increase your chances of interviewing at PharmiWeb.Jobs :
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