CRA ,

For one of our clients we are looking for an experienced CRA. You will have the ability to work directly for the sponsor, one of the top 10 pharmaceutical companies in Belgium. Together with the client, Oxford will guide & support you intensively the first months by means of coaching on the job.

Job Description

Perform all required activities to ensure appropriate monitoring of investigator sites and trial execution. Primary person responsible for management of assigned sites, including acting as central point of communication between client and Investigator sites.

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