Associate Director, Site Start-Up and Regulatory

A Leading, Global CRO are seeking to appoint an Associate Director of Site Start-up. The Associate Director Site Start-Up will assist Directors and Senior Managers in order to develop, implement and analyse work within start-up. This may include site activation, regulatory and submissions, investigator site contracts, or regulatory records. The successful candidate may also assume Project Lead responsibility for given projects and programs.

Main Responsibilities (to include but not be limited to):
+ Line Management responsibilities
+ Responsible for liaising and facilitating between Client representatives and Senior Management
+ Financial management of project support to Senior Management, as well as site start-up support
+ Responsible for facilitating and supporting project reviews with all Clinical Operations staff with regards to risk analysis, schedule, and budget
+ Oversees that customer-required project management tools and systems are efficiently implemented

Skills/Experience:
+ Educated to Degree level in Science/Life Science degree
+ Solid CRO Experience
+ Excellent experience and knowledge of Site Start-Up activities and procedures, regulations, drug development, and clinical project management
+ At Least 5 years experience of Senior Project Management/Line Management

This is a fantastic opportunity for the successful candidate to secure a permanent position within a reputable company.

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