Senior level Study Manager with Pharma background, not just CRO experiences, 5+yrs experience in Clinical Monitoring, 1-3yrs Study Management
Phases I-IV in Gout, HIV, Oncology and Inflammatory Diseases
-Solid Study Manager/CPM background and experience
-Phase II/III
-Gout ideal, others Oncology, HIV a plus
-Must have walked the shoes and have experience as a Monitor themselves and managed CROs
-Able to adapt to often change, studies evolve and change often
-Solid Contract Oversight; experience working with CROs and able to manage accountability for deliverables, timetables, and high level communication to PMs
-Drug accountability oversight/knowledge
-Attention to details, sharing info w/Clin Director, copying her on details and staying abreast of next steps
-Possible International travel, should be flexible with their schedule