Study manager

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 Comply with required training curriculum. Complete timesheets accurately as required. Submit expense reports as required. Update CV as required. Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements. 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