Associate Director, Statistics (Hybrid)

Takeda Pharmaceutical CompanyCambridge, MA
95d$153,600 - $241,340

About The Position

Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Our Data and Quantitative Sciences (DQS) is committed to harness the insight of data and digital to speed the development of highly innovative treatments to patients. These scientists (from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology, digital strategy, library sciences and data architecture/governance) bring their expertise to our global program teams and re-imagine our disciplines. They work with novel data streams, including real-world data and digital tools, and apply advanced analytics including artificial intelligence and automation. As part of DQS, the Statistics and Quantitative Sciences (SQS) at Takeda is looking to add individuals to our team that are team oriented, collaborative, exceptional leaders and innovators. SQS aspires to bring safe and effective medications to the patients with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue operational excellence.

Requirements

  • Advanced knowledge of clinical study designs, analysis methodology and data interpretation.
  • Advanced knowledge of pharmaceutical industry, overall drug development process with expertise in the cross-functional interfaces with the Statistics function.
  • Advanced knowledge of FDA and ICH regulations and industry standards applicable to the design, analysis of clinical trials and regulatory submissions.
  • Strong statistical programming skills.
  • Excellent oral and written communications skills.
  • Specialized statistical expertise in multiple therapeutic areas or development phases.
  • Strong inter-personal and people management skills.
  • Strong project management skills.
  • Strong collaborative skills and ability to work with a cross-functional team.

Nice To Haves

  • Subject matter expertise in several quantitative and statistical areas and establishes oneself as a go-to colleague on a few topics.
  • Scientific understanding of drug R&D to inform methodological input with product team or in a platform.
  • Ability to identify and research new innovative approaches and leverage fit-for-purpose methods in to programs.

Responsibilities

  • Lead delivery for one or more assets at GPT level or specialty area in clinical.
  • Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors.
  • Enable the consistent execution of the SQS and DQS seamless and predictable delivery mission.
  • Lead and be accountable for asset level delivery strategies being implemented with effective risk identification and mitigation.
  • Create an internal cross functional and external with vendors sphere of influence in predictable delivery.
  • Identify opportunity for continuous improvement in delivery approaches and leverages fit-for-purpose mitigations.

Benefits

  • Medical, dental, vision insurance.
  • 401(k) plan and company match.
  • Short-term and long-term disability coverage.
  • Basic life insurance.
  • Tuition reimbursement program.
  • Paid volunteer time off.
  • Company holidays.
  • Well-being benefits.
  • Up to 80 hours of sick time per calendar year.
  • Accrual of up to 120 hours of paid vacation for new hires.

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Industry

Chemical Manufacturing

Education Level

Ph.D. or professional degree

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