[Hiring] Biostatistician II @Parexel

Role Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities

• Operational Execution
  • Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques
  • Understand and apply moderately advanced statistical methods
  • Coordinate and lead a project team to successful completion of a project within given timelines and budget
  • Interact with clients as key contact with regard to statistical and contractual issues
  • Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
  • Check own work in an ongoing manner to ensure first-time quality
  • Provide training in statistical analysis to internal clients
  • Proactively participate in and/or lead process/quality improvement initiatives
  • Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g., discussing analysis concepts, presenting and discussing study results)
• General Activities
  • Mentor and train junior members of the department
  • Additional responsibilities as defined by supervisor/manager
• Business Development
  • Support of Business Development, e.g., by attending and preparing bid defense meetings

Qualifications

• PhD in Statistics or related discipline entry level
• MS in Statistics or related discipline with some experience
• The knowledge of pharmacokinetic data is an advantage
• Competent in written and oral English in addition to local language

Requirements

• Good analytical skills
• Good project management skills
• Professional attitude
• Attention to detail
• A good understanding of statistical issues in clinical trials
• Prior experience with SAS programming desirable
• Ability to work independently
• Good mentoring/leadership skills

Education

• PhD in Statistics or related discipline
• MS in Statistics or related discipline