As a Biostatistician at Parexel you’ll work on a variety of projects, while collaborating with our global team of experts. You’ll be able to develop your statistical skills, gain exposure to multiple therapeutic areas, become involved in business development activities, and have the opportunity to grow and develop your career within a flexible working environment. You’ll also contribute to research design and analytical strategies, provide input into protocols, and develop and review statistical analysis plans. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.
- Full Time
- Glassdoor Reviews and Company Rating
Check out the top traits we're looking for and see if you have the right mix.
"Parexel is very team oriented, so you work with a lot of people and also get to work in different therapeutic areas. There are many opportunities to find what you enjoy and the management is very supportive."James - Associate Director, Biostatistics
"Parexel is a great place to grow your career, have fun, and make a difference. Our quality-focused team culture and supportive management ensure growth, learning opportunities and achievement for every employee."Eve - Associate Manager, Biostatistics
Opportunity to learn and grow through a performance and development goal-setting program.
We value work-life balance. We try and keep regular hours and a flexible working enviroment.
Work with industry leaders and subject matter experts.
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Utilize Parexel’s industry leading clinical systems and solutions
Strong mentors with depths of experience working for global health authorities.
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 defence 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.
Good analytical skills
Good project management skills
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
PhD in Statistics or related discipline, MS in Statistics or related discipline
Recently Viewed Jobs
You have not recently viewed any jobsView all jobs