Regeneron Pharmaceuticals - Basking Ridge, NJ

posted about 1 month ago

Full-time - Senior
Basking Ridge, NJ
Chemical Manufacturing

About the position

The Associate Director Statistical Programming manages the statistical programming group within the therapeutic area(s). The incumbent oversees all activities, both internally and externally by functional service providers, related to statistical and non-statistical analysis on clinical program(s). The incumbent identifies and communicates therapeutic specific requirements and works with management to develop and implement departmental standards, applications, processes, and trainings. The incumbent represents Statistical Programming in collaboration with partnering functions and stakeholders to ensure programmer needs are met regarding therapeutic analysis specifications, application, and computing environment support. Works with management to identify resource needs based on project milestones and deliverables. The incumbent will lead process and methodology development for department goals and SME topics.

Responsibilities

  • Oversee all management functions, including internal team and external functional service providers to ensure timely and high-quality programming deliverables in assigned projects and areas.
  • Manage the implementation of programming standards, applications, processes, and trainings within the assigned area.
  • Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability.
  • Communicate and ensure commitment and reinforcement of the roles and responsibilities of the statistical/system programming function.
  • Proactive communication with study and project teams to clarify requirements and specifications, guide direct reports or support programmers on assignment status.
  • Lead and manage department goals and SME topics.
  • May oversee development of direct reports by setting goals, managing performance, evaluating and monitoring training needs, supporting development plans, mentoring, and coaching.

Requirements

  • 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
  • History of successful project and people management.
  • Expertise in one or more therapeutic areas.
  • SAS Certification desirable.

Benefits

  • Health and wellness programs
  • Fitness centers
  • Equity awards
  • Annual bonuses
  • Paid time off for eligible employees at all levels
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