Study Manager

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