CLIFYX

drug development experience, Digital Data Flow, metadata repository, clinical data standards, biometrics. We are looking for an experienced & inspiring pharma leader with hands-on expertise in Clinical Standards, Digital Data Flow, Metadata Repository, Biometrics and Data Management (EDC, non-CRF), TFLs, SDR, USDM with in-depth insights in needs, challenges and innovative trends in these domains at a global level.. Co-leads the global strategic positioning & roadmap from a business view for Clinical Standards, Digital Data Flow, Metadata Repository, Biometrics e.g. SDTM, ADaM, Regulatory Submission Packages and Data Management (EDC, non-CRF, eDTA), TFLs, SDR, USDM (e.g. STDM, ADaM.). At least 10-15 years of global drug development experience in Digital Data Flow, metadata repository, clinical data standards, biometrics, EDC, eDTA, gained preferably at top-15 pharma companies or clinical research organizations (CROs). Broad cross-pharma senior management network & preferably cross-industry forum expertise (e.g. CDISC, Transcelerate, IMI)

industry advisor

Industry Advisor Life Sciences Fulltime, Remote Life Sciences/Healthcare drug development experience, Digital Data Flow, metadata repository, clinical data standards, biometrics NY/NJ/PA/MA Preferred Northeast US Remote bonus 10-20% Job Description: Clinical - Standards and Digital Data Flow Leader Interested to be at the foreground of the next generation of clinical trials? Then this function of Clinical - Standards and Digital Data Flow Leader at  () Life Sciences (LS) might an excellent opportunity. We are looking for an experienced & inspiring pharma leader with hands-on expertise in Clinical Standards, Digital Data Flow, Metadata Repository, Biometrics and Data Management (EDC, non-CRF), TFLs, SDR, USDM with in-depth insights in needs, challenges and innovative trends in these domains at a global level. Outstanding communciation skills with ability to translate technology in a clear & easy-to-understand language and cross-pharma senior management network are fundamental to this role. Department description & Function Positioning. Life Sciences offers diverse services (e.g. clinical, IT, advisory) and Client state-of-art platform solutions (e.g. AI, IoT driven) to the life science industry. One of the platform solutions is " ADD”, a modern & open drug development platform with a wide range of offers in the clinical, regulatory and safety domain. The Clinical -Standards and Digital Data Flow Leader is part of the strategic group of Life Sciences and will work closely with ADD Product, Business Development and Marketing teams as well as multiple pharma leaders at a global level. You will be responsible for the strategic positioning, roadmap and solution development from a business perspective for Clinical - Standards and Digital Data Flow at a global level. You will drive and co-lead thought leaderships, marketing material, advisory boards and partnerships. You will support customer presentations, industry events and RFI/RFP requests of life science leaders in these domains. Main responsibilities and duties: • Contributes in building Product and solutions in Digital Data Flow, along with Product Team by providing Subject Matter expertise and knowledge on Industry Trends. • Contributes to build differentiated Product offerings to maximize Sales and increase number of customers on Product. • Co-leads the global strategic positioning & roadmap from a business view for Clinical Standards, Digital Data Flow, Metadata Repository, Biometrics e.g. SDTM, ADaM, Regulatory Submission Packages and Data Management (EDC, non-CRF, eDTA), TFLs, SDR, USDM (e.g. STDM, ADaM.) • Co-leads the design & development for these solutions from a business view • Co-leads thought leaderships and external visibility (e.g. articles, webinars, conferences, cross-industry meetings), initiates advisory boards and represents  at consortia (e.g. CDISC) • Supports business development team with customer presentations, RFI/RFP requests and go-to-market strategy. Initiates customer leaderships connects and strategic partnerships. Qualifications: • Master's degree in sciences (e.g. biology, biomedical, pharmacist, statistics) or equivalent by expertise. PhD is an advantage • At least 10-15 years of global drug development experience in Digital Data Flow, metadata repository, clinical data standards, biometrics, EDC, eDTA, gained preferably at top-15 pharma companies or clinical research organizations (CROs) • Extensive hands-on experience with Digital Data Flow, data collection standards, biostatistical programming, STDM, ADaM, TFL and regulatory submission packages, including innovative tools and strategies for automation. • Experience in applying AI in standardization, SDTM, ADaM and TFL generation. • Experience in strategy setting for generating EDC build from study protocol, SDR Model, USDM • Experience in innovative ways to automate testing and validation • Track record of building respect and trust with customers, employees and other internal and external stakeholders and partners. • Broad cross-pharma senior management network & preferably cross-industry forum expertise (e.g. CDISC, Transcelerate, IMI) • Outstanding communication skills with ability to translate technology in a clear & easy-to-understand language • Strong interpersonal skills including negotiation skills, facilitation skills and ability to drive for clarity and results when faced with ambiguity. • Fluent in English • Native German, French, Dutch or Swiss language is an advantage Travel • Travel expectations around 10% max. • Preferred locations US New Jersey, Philadelphia, Boston, Chicago or San Francisco/California region • Other locations are also possible.

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