Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Senior Biostatistician
Job ID R0000002323 , RemoteKey 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 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.
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:
PhD in Statistics or related discipline, MS in Statistics or related discipline
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