Description
Primary Responsibilities:- Responsible for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget
- Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor
- Provide input to the study budget and is responsible for managing assigned vendor budgets
- Identify and track timelines, milestones, critical study activities, issues and budget and provide regular updates to the Study Team and Clinical Program Leader (CPL) as appropriate
- Conduct protocol and site feasibility assessments
- Provide input to the program budget and is accountable for managing overall study budget where assigned
- Delegate and oversee study activities assigned to Clinical Operations Study Team as applicable
Skills / Experience:
* Experienced in clinical trial management (4+ years)
* Experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, conduct and monitoring of clinical studies
* Familiar with global trial requirements
* Demonstrated creativity and innovation to support projects and initiatives
* Excellent planning and organizational skills
* Flexible and solution focused
* High level of initiative and ability to work independently
* Strong analytical skills
* Strong customer focus
* Highly effective verbal and written communication skills in English
Education: Bachelors degree or equivalent undergraduate degree (scientific or healthcare discipline preferred)
To find out more about Real please visit www.realstaffing.com