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