[Hiring] Senior Biostatistician @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

• Coordinate and lead a project team to successful completion of a project within timelines and budget.
• Interact with clients as key contact with regard to statistical and contractual issues.
• Perform QC of derived datasets, tables, figures and data listings produced by other members of the department.
• Check own work in an ongoing way to ensure first time quality.
• Understand and apply advanced statistical methods.
• Lead production and quality control of randomizations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
• Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review.
• Travel to, attend, and actively contribute to all kinds of client meetings as appropriate (e.g. discussing analysis concepts, presenting, discussing and interpreting study results).

Business Development

• Support of Business Development, e.g. by actively contributing to study design considerations in internal and client meetings.
• Providing and discussing sample size scenarios.
• Support of budget and proposal development.
• Attending and preparing bid defense meetings for potential studies, programs of work and FSPs.

General Activities

• Additional responsibilities as defined by supervisor/manager.

Qualifications

• PhD in Statistics or related discipline with some experience or MS in Statistics or related discipline with significant 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.
• Thorough understanding of statistical issues in clinical trials.
• Prior experience with SAS programming required.
• Ability to work independently.
• Good leadership skills.
• Good business awareness/business development.
• Willingness to work in a matrix environment and to value the importance of teamwork.

Education

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