Biostatistician II (FSP)

<p><b>When our values align, there&#39;s no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world&#39;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.</p><p>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&#39;re committed to making a difference.</p><p></p><p></p><p><b><u><span>Key Accountabilities</span></u></b>:</p><p><b>Operational Execution</b></p><ul><li>Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques</li><li>Understand and apply moderately advanced statistical methods</li><li>Coordinate and lead a project team to successful completion of a project within given timelines and budget</li><li><span>Interact with clients as key contact with regard to statistical and contractual issues</span></li><li>Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents</li><li>Check own work in an ongoing manner to ensure first-time quality</li><li>Provide training in statistical analysis to internal clients</li><li>Proactively participate in and/or lead process/quality improvement initiatives</li><li>Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results</li></ul><p></p><p><b>General Activities</b></p><ul><li>Mentor and train junior members of the department</li><li>Additional responsibilities as defined by supervisor/manager</li></ul><p></p><p><b>Business Development</b></p><ul><li>Support of Business Development, e.g. by attending and preparing bid defense meetings</li></ul><p></p><p><b>Skills:</b></p><ul><li><span>Good analytical skills</span></li><li><span>Good project management skills</span></li><li><span>Professional attitude</span></li><li><span>Attention to detail</span></li><li>A good understanding of statistical issues in clinical trials</li><li><span>Prior experience with SAS programming desirable</span></li><li><span>Ability to work independently</span></li><li><span>Good mentoring/leadership skills</span></li></ul><p></p><p><b><u>Knowledge and Experience</u></b>:</p><ul><li>PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience</li><li>The knowledge of pharmacokinetic data is an advantage</li><li>Competent in written and oral English in addition to local language</li></ul><p></p><p><b><u><span>Education: </span></u></b></p><ul><li>PhD in Statistics or related discipline, MS in Statistics or related discipline</li></ul>