Job Description
Responsibilities
- Perform monitoring visits according to monitoring plan (including trial initiation, training and closeout activities)
- Participate in site nomination process, perform evaluation of site capability and make recommendation for inclusion in clinical trial
- Point of contact for sites and facilitator of communication between sites and key line functions
- Ensure preparation, collection and distribution of trial master file documents and maintenance of investigator site file
- Timely write-up of study monitoring visit reports
- Set up and ensure maintenance of investigator site file
- Manage site vaccine supply and sample management during course of study
- Ensure site performance in line with milestones and KPI’s (i.e. start-up, recruitment, closeout, etc.)
- Support investigator in implementing appropriate contingency plans as needed
Requirements
- A first experience as CRA
- Master degree in science related field
- Knowledge of Office
- Strong verbal communications skills
- Good cooperative and collaborative skills
- Dutch/English/French knowledge