Associate Director, Biostats

🕒 il y a 8 mois

🏖️ New Jersey – Distant

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💵 $146 640 - $219 960 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

🦅 Parrain de Visa H1B

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👻 Score fantôme 35%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Genmab

Genmab

1001 - 5000 employés

Fondée en 1999

🏥 Santé

🧬 Biotechnologie

💰 €134 000 000 Post-IPO Equity en 2010-06

Healthcare • Biotechnology

Genmab est une entreprise de biotechnologie dédiée à la transformation des vies grâce à une science des anticorps pionnière. L'entreprise s'engage à développer des thérapies innovantes à base d'anticorps pour diverses maladies, dans le but d'améliorer les résultats pour les patients et les options de traitement. Les efforts de Genmab en matière de recherche et de développement d'anticorps soulignent son engagement à faire progresser la science médicale.

Description

• Act as lead and main point of contact related to Statistics for designated compound/indication • Follow scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation and improve efficiencies • Engage with regulatory authorities on compound/indication level discussions • Ensure consistency of statistical methods and data handling across trials • Ensure all compound/indication related work and information is shared between biostatisticians involved in the compound and with the vendor • Provide scientific advice to the CDT including design of trials, analyses and analyses requiring advanced statistical methodologies/techniques • Represent the CDT/the company at regulatory meetings, during Key Opinion Leaders meetings, network and/or Partner meetings, as applicable • Ensure availability of integrated database(s), as needed, and planning and conduct of integrated analysis to support development decisions, submissions, and marketing needs • Support development and communication in relation to communication strategy and/or scientific input to presentations, posters, and articles • Engage with regulatory authorities on trial level discussions • Coordinate data transfers from/to business partners in collaboration with the programmer and the data manager, as applicable

🎯 Exigences

• Master's or PhD in a statistical discipline • 8+ years of experience in relevant area preferred, or demonstrated capability • Experience in statistical analysis, modelling and simulation and adaptive trial designs • Experience with drug development in biologics, targeted therapies, and companion diagnostics preferred • Experience working with FDA, EMA, and ICH guidance for drug development pertaining to statistics • Experience with the relevant regulatory requirements for biostatistics processes and SOPs • Experience with regulatory submissions including BLAs and previous experience in dealing with Health authorities such as discussions/negotiations in filing strategies • Experience working with SDTM, ADaM, eSUB, and CDISC requirements for regulatory submissions • Experience directing multiple complex projects/studies in a technical capacity • Proven performance in earlier role/comparable role

🏖️ Avantages

• 401(k) Plan: 100% match on the first 6% of contributions • Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance • Voluntary Plans: Critical illness, accident, and hospital indemnity insurance • Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave • Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support • Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

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