Our Client is a rapidly growing international Clinical Research Organisation offering an experienced (Senior) CRA opportunity to work from home on full FTE as part of their team in Italy.
Responsibilities:
- Conducting start-up activities and monitoring visits
- Maintaining study files, writing clinical trial reports and liaising with vendors
- Reviewing progress of projects and initiating appropriate actions to achieve objectives
- Participation in the development of protocols and Case Report Forms
- Liaising with CPM to evaluate needs, resources and timelines
Requirements:
- Minimum 3 years of on-site monitoring experience
- Preferred experience in Oncology clinical trials
- Ability to travel as needed to support project requirements
- Degree or equivalent in a life science discipline
- Fluency in English and Italian
- Strong communication and team work skills
The company offers an attractive package and dynamic work environment. To apply for this role, please send your CV to joanna.osiak@pharmaprofessionals.eu