Lead Statistical Sas Programmer, Oncology, Single Sponsor
hace 2 semanas
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.As a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex oncology projects for a renowned, innovative and global top pharmaceutical company.Our sponsor is looking for Lead Statistical Programmers capable of overseeing studies from the Pharma side.You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics.This may be for either in-house programmed or out-sourced studies in either their Early or Late Phase team. It is a great opportunity to see more how this works from a Big Pharma perspective, whilst still being part of a global CRO with opportunity for future career growth.The decision you make today could change the future of our patients tomorrow. Join us at Fortrea. Stand at the forefront of Oncology research.You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country.What else can you expect from us?Rewarding and meaningful work in an established, diverse, highly profitable and respected global companyHighly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.A genuine work-life balanceFlexibility in working hoursA thorough onboarding with support from your personal mentorA permanent employment contract with FortreaExcellent training and career development opportunities, as well as support with advancing your individual educationStrong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwideMain Responsibilities:Plan, execute and oversee all programming activities on a study, including but not limited to resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc.Oversee SDTM, ADaM and TLF development, perform Senior Review of outputsLiaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analysesSupport / oversee submission activities (especially in late phase team)Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all timesMentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processesYour profile:Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical companySolid experience with complex oncology clinical trials (minimum 5 years) and the corresponding datasets’ content (safety and efficacy) and endpointsLead experience in Oncology trials (from pharma or CRO perspective)Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data ManagementExpert knowledge of base SAS, SAS macros, SAS / STAT and in debugging SAS programsBroad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guides and submission standardsAn autonomous, collaborative work style, a curious mind and a keen attention to detailFluency in English both verbal and written is a mustREMOTELI-AA3Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.J-18808-Ljbffr
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España MAI Fortrea Development Limited A tiempo completoAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Statistical Programmer CVRM
hace 1 mes
España AstraZeneca A tiempo completoLOCATION: Barcelona office (3 days office – 2 working from home)About CVRMAt AstraZeneca CVRM Biometrics we work on a wide range of agile and innovative projects within the Cardiovascular, Renal and Metabolism therapeutic area, providing solutions and treatments for millions of patients across the globe.About the RoleWe are now looking for an experienced...
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Statistical Programmer II
hace 4 semanas
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Senior Statistical Programmer
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España buscojobs España A tiempo completoThe Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions, working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.IQVIA Biostatistics helps interpret and draw inferences from data...
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Sr. Statistical Analyst Programmer
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Senior Statistical Programmer
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España ICON plc A tiempo completoPrincipal Statistical Programmer - EMEA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Location: Homebased (UK, South Africa, Poland, Spain,...
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España IQVIA A tiempo completoJoin us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions, working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps...
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Sr Statistical Programmer
hace 2 semanas
España Syneos Health A tiempo completoDescriptionSenior Statistical ProgrammerSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the...
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Sr Statistical Programmer
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Sr. Statistical Analyst Programmer
hace 24 horas
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hace 1 mes
España INSUD PHARMA, S.L.U. A tiempo completoOverview: We are seeking a highly skilled and experienced Senior Clinical Data Programmer to join our dynamic team. The successful candidate will be responsible for overseeing the programming and validation of clinical trial databases, ensuring data accuracy, integrity, and compliance with regulatory standards. This role requires a strong background in...
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Senior Statistical Programmer
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España AstraZeneca A tiempo completoThe Senior Statistical Programmer I is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex...
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hace 3 semanas
España AstraZeneca A tiempo completoThe Senior Statistical Programmer I is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex...
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Senior Statistical Programmer
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España AstraZeneca A tiempo completoThe Senior Statistical Programmer I is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex...
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hace 1 mes
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Senior Statistical Programmer, Early Phase
hace 1 semana
España buscojobs España A tiempo completoWhy IQVIA DSSS?Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership.This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor...
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Senior Statistical Programmer, Early Phase
hace 1 mes
España IQVIA A tiempo completoWhy IQVIA DSSS? Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor...
