Study Manager

**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:**  **General Accountabilities**  • Build and maintain engagement with Investigators, other site staff in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out.  • Ability to manage studies and processes to agreed quality and timelines.  • Ability to proactively identify & mitigate risks around study/site level in study execution.  • Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies.  **Compliance with Parexel standards**   • Complies with required training curriculum   • Completes timesheets accurately as required   • Submits expense reports as required   • Updates CV as required   • Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements  **Skills:**   • Previous experience in scientific and/or regulatory medical writing.  • Strong Communication Skills  **Knowledge and Experience:**  • Keen problem-solving skills.  • Fluent in both oral and written English.  • Fluent in host country language required.  • At least 5 years in clinical practices  **Education:**   • Minimum of BS/BA in a biomedical discipline or equivalent education/training is required