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
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