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.

CRA:

Knowledge and Experience: 

• At least 1.5 years (2 years preferable) of Clinical Monitoring/ Site Management experience, global study monitoring experience is preferred 

• Good knowledge of ICH/GCP, relevant international and local regulations relating to Clinical Research 

Education:  

• Degree in Life Science, Pharmacy, or other relevant education background 

• Bachelor’s degree or above, or equivalent 

Study Manager:

Knowledge and Experience: 

• Minimum of BS/BA in a biomedical discipline or equivalent education/training is required.

• At least 7 years in clinical practices.

• Good working knowledge of Good Clinical Practices (GCPs), monitoring, clinical drug development process and country regulatory environment.

• Experience with clinical research methodology (e.g., study design, study monitoring and data

analysis). Prior study management and/or study coordination experience preferred.

• Demonstrated effectiveness in working in a multidisciplinary, matrix team situation.

• Advanced education and/or training/experience desirable.

Education:  

• Degree in Life Science, Pharmacy, or other relevant education background 

• Bachelor’s degree or above, or equivalent