Senior Manager Statistical Programming

Leiden, Netherlands
20 Nov 2018
13 Feb 2019

Senior Manager Statistical Programming


We are working with a world leading pharmaceutical company that is passionate about discovering and developing innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases.

They are looking for talented people who share their vision for reshaping how healthcare is delivered, managed and experienced, and who believe that nothing can’t be solved when committed individuals bring together their resources and their resolve.

They offer:

  • Competitive salary
  • Annual bonus up to 9%
  • Very competitive benefits package including a Career Average Earnings pension, medical cover, share scheme and childcare vouchers
  • Excellent career development opportunities

This position plays the role of both project and people leader within statistical programming. As a project leader you will be responsible for formulating the programming strategy of one or more programs, providing operational oversight and you will be accountable for the planning and execution of statistical programming  activities across multiple studies.

As a people leader you will have line management responsibility and be responsible for recruitment, onboarding, performance management and people development as applicable. You will also be accountable for effective resource allocation and utilization of resources.

Personal Requirements:

  • In-depth knowledge of SAS statistical software.
  • Proven project management experience dealing with customers, leading teams to successful outcomes, outsourcing strategies, contract oversight, and negotiations.
  • Excellent leadership, decision-making skills and proven ability to foster team productivity and cohesiveness and act as a change agent.
  • Experience working on cross-functional teams
  • Demonstrated innovative thinking to allow for optimal design and execution of clinical development strategies.
  • In-depth knowledge of regulatory guidelines and publishing processes.

Please do not apply if you do not have the skill(s) we require as we cannot consider the application if you do not meet the requirements.

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