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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 R0000021499 Bengaluru, Karnataka, India

Job Purpose:

The Senior Biostatistician works independently in the production and quality control of analysis plans, reports, derived datasets, tables, listings and figures, provides statistical advice to clients and fulfils the project primary role within a designated project team.

Operational Execution:

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 kind of client meetings as appropriate (eg discussing analysis concepts, presenting, discussing and interpreting study results)

Business Development:

Support of Business Development, eg 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.

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

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

Knowledge and Experience:

 · 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 Education:

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