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  

• 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