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SITE ACTIVATION SPECIALIST - CLINICAL REGULATORY

Posted on Mar 16, 2019 by HAYS

Brussel, Brussel Belgium
Research & Development
Immediate Start
Annual Salary
Full-Time
Hays Wavre * Trial start-up * CEC and CA submissions * Belgium For one of its clients, Hays Life Sciences is Recruiting a Clinical Regulatory Specialist with at least three years of experience in Site Activation Regulatory operations completing CEC and CA submissions. As a Site Activation Specialist, you will manage the preparation, review and coordination of Country Submissions (MoH, EC and additional special national local applications) in line with global submission strategy. You will provide, under guidance, local regulatory strategy advice (MoH &/or EC) to internal clients and will provide project specific local SIA services and coordination of these projects. You may have contact with investigators for submission related activities and will play a key-contact role at country level for either Ethical or Regulatory submission-related activities. You will coordinate with internal functional departments to ensure various site start-up activities are aligned with submissions activi...

Reference: 672228759