Support CSM staff in start up activities such as (but not limited to) country and site feasibility
Support CCOM, Senior COM and other functional areas to develop and support implementation of a
Support the strategy and development surrounding country and site activation planning inclusive of
Collect and analyze AbbVie and industry (as available) benchmarking data across assigned disease
Liaison cross-functional staff on use of templates and systematic processes for study start up
Track progress against study start up timelines and milestones and escalate risks to CCOM and

🎯 Requirements

Education: Bachelor OR Master Degree, health related (e.g. Medical, Scientific, Nursing, Pharmacy)
At least 2 years experience as a people manager or project manager
CRA background and knowledgeable for the life cycle of clinical trials
Familiar with SSU activities
Familiar with HGRAC management
Strong personality of result driven

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