MidFull TimeENAsia/Pacific
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
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