Responsible for study management aspects of assigned studies, including vendor and budget management.
Regional/Country/Study level implementation of Startup and Site Activation Plans.
Responsible for regional/country/study level Recruitment Strategy.
Support the development of study level plans.
Communication with the local team and internal stakeholders and CRO partner as applicable to ensure efficient and timely study delivery of the agreed plans.
Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables.
Requirements
Minimum of 5 years of relevant regional clinical trial management experience.
Recent strong experience in ICD customization at local level.
Recent strong experience in leading local team.
Excellent leadership, communication, and organizational skills.
Able to multi-task under limited direction and on own initiative.
M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential
Prior and demonstrable experience working at a senior level within Study start up