Description
Main Responsibilities:Develop and oversee all aspects of the conduct of clinical studies in accordance with GCP. Develop protocols, critical study documents and project plans; Identify and recruit qualified sites; Oversee site activities including training and adherence to study plans and milestones; Oversee regulatory compliance and data management.
Previous experience developing relationships with key investigators, selecting vendors and managing vendor relationships and delivering results on schedule. Ability to build strong cross-functional relationships, excellent presentation skills, and strong verbal communication skills. Previous Diagnostic experience strongly preferred.
Education/Experience:
Must have 6-10 years clinical trial management experience, preferably in diagnostics, including clinical study management, site management, knowledge of product development regulatory requirements, experience with multi-project planning and coordination, and budgeting and forecasting. Must have 4 year college degree, Life Sciences preferred.
To find out more about Real please visit www.realstaffing.com