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.
Required Qualifications:
• Study design expertise, specifically for IIT and RWE studies
• Protocol development experience
• Proficiency in SAS and R programming
• Excellent communication skills with relevant stakeholders
• Available for interviews soon
Company
Parexel designs and delivers clinical trial solutions across Phase I–IV, combining clinical, regulatory, and therapeutic expertise to accelerate drug development with a patient-first mindset.
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