Associate Director, Site Start Up and Maintenance
vor 1 Woche
Description The Associate Director, Site Start-Up and Maintenance plays a pivotal leadership role within the global clinical operations team. This position is responsible for overseeing the strategic planning and execution of global site regulatory, budgeting, and contracting maintenance activities. The role ensures the delivery of high-quality, timely site maintenance services by collaborating closely with internal and external stakeholders. TheAssociate Director, Site Start Up and Maintenanceis responsible forline management of assigned staff, as well as defining, developing, and delivery of the global siteregulatoryand site budgeting and contracting maintenancetasks,by partnering withinternal and externalstudyteammembers. Provide guidance to staff and oversee the analysis of clinical trial intelligence data and its application to effectively conductaccurateand effectiveresourcingforecasts, robustplanning, andon time delivery ofsitemaintenance tasks. Directly support priority orhighly complexprojects through study closure. Champion thecreationandimplementationof innovativeprocesses,methodologies, data andtechnologiesthatwillensureongoingdelivery ofvaluedsite startup and sitemaintenanceservices. Responsible for line management, mentoring, and development of assigned staff Accountable for defining, developing, and delivery ofsitemaintenance tasks Partners with CRO's, Clinical Operations teams, and TAU partners to improve overall metrics and implement processes Provides guidance, oversight, and training to theSiteStartUpand Maintenance Teams, delivering activities in support of Clinical Programs, including data and methodologies forefficient and effectivesite maintenanceplanning, and modeling Ensures consistent standards are applied to thesite maintenanceprocess across project portfolios and supports continuous improvement activities while developing and implementing TA-aligned strategies / approaches Drives the creation and implementation of innovative solutions to improve processes and acceleratesite maintenancetimelines Leverages leading industry tools and data sources to provide data on timelines and performance toassiststudyteams with studysitemaintenancetimeline forecasting Agrees to deliverables on a country and site-level basis with thestudy teamandmonitoradherence to these. Promptly recognize and remediate potential delays, and escalate non-performance as needed. Leads the cross-functional sitemaintenanceteam,utilizingtheappropriate teammembers to support thestudysite maintenancerequirements Serves as point of escalation andassistsin resolution of issues Act as a role model for Takeda’s values BS degree or international equivalent in a life sciencerequired, advanced degree preferred Extensive experience (≥ 8 years) in Clinical Operations, Project Management, study start-up,site budgeting and contractingand / or trial optimization with evidence of increasing responsibility within a pharmaceutical company, CRO orrelevantindustry vendorrequired More than 5 years of direct responsibility in site management and oversight of the site maintenanceprocesses of clinical research studies at a sponsor or CRO Expertisein clinical trial regulations and ethics committee submissions Expertisein site contract and budgetamendments administration Expertisewith leading edge trial optimization vendors, tools, and methods Experience in line management and workingin amatrixenvironment Proficiencywith software models and database structures Expertiseinprinciplesdriving sitemaintenancestrategiesincluding site contract amendments Direct experience in the pharmaceutical industry or related fieldrequired Ability to stronglydemonstrate, interpret, explain, represent, and drive unbiased data insights into clinical trials operationaldelivery Ability to develop deep insights, uncover unmet needs, drive innovation, inspire, develop,collaborateand lead within a global matrixed team Ability to explain data,facilitatedecision making processes to be data driven Locations Zurich, SwitzerlandWorker Type EmployeeWorker Sub-Type RegularTime Type Full time
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Associate Director, Site Start Up and Maintenance
vor 2 Wochen
Zürich, Schweiz Takeda VollzeitAssociate Director, Site Start Up and Maintenance Join to apply for the Associate Director, Site Start Up and Maintenance role at Takeda The Associate Director, Site Start-Up and Maintenance plays a pivotal leadership role within the global clinical operations team. This position is responsible for overseeing the strategic planning and execution of global...
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Associate Director, Site Start Up and Maintenance
vor 2 Wochen
Zürich, Schweiz Takeda VollzeitDescription The Associate Director, Site Start-Up and Maintenance plays a pivotal leadership role within the global clinical operations team. This position is responsible for overseeing the strategic planning and execution of global site regulatory, budgeting, and contracting maintenance activities. The role ensures the delivery of high-quality, timely site...
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Global Site Start-Up
vor 2 Wochen
Zürich, Schweiz Takeda VollzeitA global biopharmaceutical company in Zurich is seeking an Associate Director for Site Start Up and Maintenance. This pivotal role involves leading a team to execute global site regulatory, budgeting, and contracting maintenance activities. The ideal candidate will manage staff, guide project support, and innovate processes to enhance site maintenance...
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Zürich, Schweiz Takeda VollzeitAssociate Director, Drug Product Manufacturing Science & TechnologyJoin to apply for the Associate Director, Drug Product Manufacturing Science & Technology role at Takeda.1 day ago – Be among the first 25 applicants.About the roleAs Associate Director, Drug Product Manufacturing Science & Technology, you will be Takeda’s global subject matter expert for...
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Associate Director
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Zürich, Zürich, Schweiz Elixion Biotech VollzeitWe are seeking an Associate Director or Director – Systems/Computational Biologist for Drug Discovery to lead advanced computational biology initiatives at the intersection of quantum physics, systems biology, and Network medicine. This role partners closely with biology, chemistry, and data science teams to convert complex multi-omics and...
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Associate Director, Project Management
vor 2 Wochen
Zürich, Zürich, Schweiz MSD Vollzeit $ 139'600 - $ 219'700Job DescriptionGlobal Project and Alliance Management (GPAM) sits in the R&D organization at our Company. GPAM comprises several distinct groups, including Project Managers in Value & Implementation (which is this job), Development, and CMC; Discovery Portfolio Managers; Alliance Managers; Project Management Office (PMO); and Administrative...
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Associate Director, Global Market Access
vor 2 Wochen
Zürich, Schweiz 1008 Vifor Pharma Management Ltd. VollzeitA leading global pharmaceutical company is looking for an Associate Director Market Access to develop strategies ensuring timely access to innovative therapies. You will lead cross-functional teams, implement pricing solutions, and navigate healthcare systems. The ideal candidate has 8-10 years of experience in market access or pricing within healthcare, and...
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Associate Director, Project Management
vor 1 Woche
Zürich, Zürich, Schweiz MSD Vollzeit $ 142'400 - $ 224'100Job DescriptionPosition Description/Summary:The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders to develop strategies and execute our Company's drug and vaccine V&I efforts to progress the R&D pipeline and realize its full potential.The Associate...
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Zürich, Zürich, Schweiz Takeda VollzeitBy clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...
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Associate Director, API Process Engineering
vor 2 Wochen
Zürich, Schweiz Takeda VollzeitDescription About the role As Associate Director, API Process Engineering, you will be Takeda’s global expert for small-molecule API manufacturing processes across batch and continuous platforms. You will apply chemical engineering and process chemistry fundamentals to design, scale, and control API processes from clinical development through commercial...