Offer summary
Qualifications:
Bachelor's degree in a relevant field, Experience in clinical studies.Key responsabilities:
- Coordinate operational aspects of studies
- Review data management deliverables and study documentation
Description:
Lead and coordinate activities that ensure quality, consistency, and integration of study data and progress operational deliverables to time cost and quality objectives from Study Specifications (SS) through study close-out activities and Clinical Study Report (CSR). Work with and lead cross-functionality, with internal and external partners, on global studies across different phases of drug development and different therapy areas.
Accountabilities/Responsibilities:
Minimum Requirements –Education and Experience
Skills and Capabilities
Leadership Capabilities at level 2
Internal and External Contacts/Customers - Some examples of contacts/customers are:
Date Posted
01-8月-2017Closing Date
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