Description
The Clinical Trial Manager is responsible for managing the operational implementation of studies to support the development and commercialization of novel assays which lead to improved treatment decisions for oncology patients.Responsibilities:
- Monitor study progress from study initiation through publication of study results, including maintenance of the study timeline; execution of tasks by functional area; regulatory and protocol compliance
- Develop working knowledge of GHI study initiation, execution, analysis and closing procedures; study-related documentation; and study, program and business goals and milestones
- Coordinate and maintain effective collaborator communications for specimen tracking, study conduct and/or data review, to include but not limited to periodic teleconferences and face-to-face meetings
- Identify potential problems and issues; prioritize relative to program and business goals; escalate to program leadership if appropriate
- Creates study-specific files; collects and maintains all required documentation and correspondence
Requirements:
- Bachelor's degree in life sciences, scientific or other relevant discipline
- 2-4 years related experience in the health care, biotechnology or diagnostics industry
- Familiarity with Microsoft tools, specifically Word; Excel; PowerPoint; and Project
- Demonstrated ability to deliver quality results in a timely manner
- Comfortable to be in a fast-paced, rapid growth environment
To find out more about Real please visit www.realstaffing.com