Unknown Company

Director, Statistical Programming

madison, nj • Posted 5 days ago
Onsite Full Time Risk Management & Quantitative Analysis

Director, Statistical Programming

Responsibilities

  • Provide technical leadership for portfolio delivery and ensure Statistical Programming delivery with high quality and efficiency.
  • Act as Cluster Head: create and implement delivery strategies for seamless project delivery.
  • Lead statistical programming activities across an indication/disease area, ensuring quality and timeliness.
  • Set tasks and prioritization across the indication/disease area; engage cross-functionally to progress work.
  • Lead recruitment and retention strategies for Statistical Programming in collaboration with Statistical Programming LT, HR, and Talent Acquisition.
  • Lead indication/disease-area level statistical programming strategies.
  • Provide comprehensive programming leadership and support to complex clinical project teams and vendors, including deployment of programming strategies, standards/specifications, and programmed analyses to comply with regulatory requirements, SOPs, and work practices.
  • Provide guidance on innovative strategies/technologies for clinical trial programming at program level.
  • Lead process improvement initiatives and drive efficiency; challenge status quo as appropriate.
  • Member of Extended Statistical Programming Leadership Team.
  • Functional management/people leadership: set objectives, manage performance, coach/feedback; support evaluation and recruitment.

Minimum Requirements

  • MS with ~10+ years industry experience.
  • BS with ~12+ years industry experience.
  • Proven track record of leading business process transformations and organizational culture change; driving programming expertise on complex deliverables.
  • Proven track record of attracting and retaining talent.
  • Pharmaceutical drug development operational experience with significant direct exposure to clinical development.
  • Health care business acumen and comprehensive understanding of the pharmaceutical industry.
  • Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical concepts, and medical terminology used in analysis/submission.

Benefits (explicitly stated)

  • Health coverage (medical, pharmacy, dental, vision); wellbeing support; financial wellbeing/protection (401(k), disability, life insurance, accident insurance, supplemental health, business travel protection, personal liability, identity theft benefit, legal and survivor support).

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Director, Statistical Programming in madison at Unknown Company

This position is listed as full time and onsite.

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