Offer summary

Qualifications:

PhD or MS in Statistics or related discipline., Good understanding of statistical issues in clinical trials., Prior experience with SAS programming is desirable., Competent in written and oral English, with good analytical and project management skills..

Key responsabilities:

Produce and QC derived datasets and statistical outputs using programming techniques.

Coordinate and lead project teams to ensure timely and budget-compliant completion.

Interact with clients regarding statistical and contractual issues.

Mentor and train junior members of the department and support business development activities.

Job 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

Operational Execution:

Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques
Understand and apply moderately advanced statistical methods
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
Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Check own work in an ongoing manner to ensure first-time quality
Provide training in statistical analysis to internal clients
Proactively participate in and/or lead process/quality improvement
initiatives
Travel to, attend and actively contribute to all kind of client meetings as appropriate (eg discussing analysis concepts, presenting and discussing

study result

General Activities:

Mentor and train junior members of the department
Additional responsibilities as defined by supervisor/manager

Business Development:

Support of Business Development, eg by attending and preparing bid defense meetings

Skills:

Good analytical skills
Good project management skills
Professional attitude
Attention to detail
A good understanding of statistical issues in clinical trials
Prior experience with SAS programming desirable
Ability to work independently
Good mentoring/leadership skills

Knowledge and Experience:

PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience
The knowledge of pharmacokinetic data is an advantage
Competent in written and oral English in addition to local language

Education: