Senior Biostatistician - FSP

Actively Reviewing

Parexel

4–8 yrs exp Posted 3 months ago

Job Description

Key Accountabilities

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
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.
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
Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results)
Additional responsibilities as defined by supervisor/manager.

Skills

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 skills
Willingness to work in a matrix environment and to value the importance of teamwork.

Knowledge And Experience

PhD in Statistics or related discipline with 3+years of experience or MS in Statistics or related discipline with 5+ years of experience
Competent in written and oral English in addition to local language

Education: