Associate Director, Biostatistics

🕒 il y a 1 mois

🇺🇸 États-Unis – Télétravail

💵 $189 670 - $229 834 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

🦅 Parrain de Visa H1B

Cette entreprise a parrainé des visas H1B par le passé.

👻 Score fantôme 13%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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Bristol Myers Squibb

Site WebLinkedInTous les Emplois

10 000+ employés

Fondée en 1887

🏥 Santé

💼 Conseil

📦 Logistique

Healthcare • Consulting • Logistics

Bristol Myers Squibb est une entreprise biopharmaceutique mondiale engagée dans la découverte, le développement et la distribution de médicaments innovants qui aident les patients à surmonter des maladies graves. Leurs domaines de prédilection incluent la santé cardiovasculaire, la thérapie cellulaire, l'immunologie et l'oncologie. Avec un engagement à transformer les résultats pour les patients grâce à une science de pointe, Bristol Myers Squibb collabore avec un réseau mondial de chercheurs, de prestataires de soins de santé et d'autres parties prenantes. Ils visent à être des leaders dans l'innovation pour les patients tout en favorisant la diversité et l'inclusion au sein de leur personnel.

Description

• Serve as the lead biostatistician for clinical oncology projects, developing and executing statistical strategies, study designs, and analyses. • Collaborate with multidisciplinary project teams to ensure timely communication and alignment of objectives. • Identify and implement solutions to statistical and data analysis issues related to clinical trials and regulatory submissions. • Author and own key statistical documents and outputs, including protocol statistical sections, SAPs, and TLF shells. • Review study-related documents and validate vendor deliverables, including CDISC data specifications and TLF/analysis outputs. • Work with internal programmers to support regulatory requests, DSUR/IB updates, and ad-hoc analyses. • Participate in internal sponsor review of ongoing clinical data. • Explore and pilot AI initiatives that enhance quality control and operational efficiency. • Travel approximately 10% of the time. • Perform occasional evening and weekend work.

🎯 Exigences

• Advanced degree in Statistics or Biostatistics (PhD or MS) • 8+ years of biostatistics experience in the pharmaceutical/biotech industry with a PhD, or 10+ years with an MS • Experience utilizing AI-enabled tools to improve productivity and work efficiency • Familiarity with statistical programming tools such as SAS and/or R • Working knowledge of CDISC standards (SDTM/ADaM) • Ability to review and interpret key statistical outputs • Ability to oversee vendors and ensure quality, timeliness, and compliance of biometrics deliverables • Solid understanding of GCP, ICH guidelines, and regulatory requirements • Excellent interpersonal and communication skills, with ability to influence cross-functional stakeholders • Ability to function in a highly regulated environment and adhere to RayzeBio guidelines and SOPs • Prior experience in oncology clinical development preferred • Prior experience with global regulatory submissions preferred • Willingness to travel approximately 10% of the time • Availability for evening and weekend work

🏖️ Avantages

• Additional incentive cash and stock opportunities (based on eligibility) • Medical, pharmacy, dental, and vision care • BMS Well-Being Account • BMS Living Life Better • Employee Assistance Programs (EAP) • 401(k) plan • Short- and long-term disability • Life insurance • Accident insurance • Supplemental health insurance • Business travel protection • Personal liability protection • Identity theft benefit • Legal support • Survivor support • Flexible time off (unlimited, with manager approval) for US Exempt Employees • 11 paid national holidays for US Exempt Employees • 160 hours annual paid vacation for Phoenix, AZ, Puerto Rico and RayzeBio Exempt, Non-Exempt, Hourly Employees • 11 national holidays and 3 optional holidays for Phoenix, AZ, Puerto Rico and RayzeBio Exempt, Non-Exempt, Hourly Employees • Unlimited paid sick time, based on eligibility • Up to 2 paid volunteer days per year, based on eligibility • Summer hours flexibility, based on eligibility • Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs • Annual Global Shutdown between Christmas and New Years Day • Reasonable workplace accommodations/adjustments and ongoing support