About this role
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