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

• 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