International research-focused pharmaceutical company with over 85 years experience is looking for a Clinical Trial Transparency & Documentation Specialist to contribute to the implementation and maintenance of the Clinical Trial Disclosure requirements and to act as EDMS Subject Matter Expert and Key User for the GCD Department, supporting the management activities for clinical studies documentation, throughout documents life-cycle and system maintenance.
Our client is operating in 30 countries with more than 6,000 employees and their R&D team represents a fundamental asset for the business.
You would join a dynamic, fast-growing, challenging and friendly environment in a company that firmly believe that their people are their most valuable asset, that is why they invest in continuous training, learning and development.
The job is an internal substitution which means you will have great opportunities of career development.
Responsibilities:
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