Clinical Research Associate

Company Name: PPD Development (S) Pte Ltd
Tokyo, Tokyo, Japan

Skill Level: Mid Level

Categories: Associate, Other

Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Responsible for ensuring that data will pass international quality assurance audits. Develops collaborative relationships with investigational sites.

Education and Experience:  (Required education, training, licenses, accreditation or certification and quantity and type of directly related experience. In many cases an “equivalency,” consisting of a combination of education and prior directly related experience, is sufficient for the individual to perform the job satisfactorily.)

 ·       Bachelor’s degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution.  In some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered. ·       Valid Driver’s License where applicable·       Minimal clinical monitoring experience that provides the required knowledge, skills, and abilities.  In some cases previous experience in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care OR experience in a health sciences field with formal training in medical terminology and anatomy may be considered.  

Contact Information:
Goh Woei Woei
Phone: +65 63029554

woeiwoei.goh@ppdi.com
http://www.ppdi.com

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