Can you see yourself in a position where you can use your experience to coach more junior CRAs? This client is looking for a freelance CRA to support their team and training CRAs is an integral part of the role. You will mainly be working on oncology and complex trials in this position, so you will be very close to the scientific aspect of clinical trials, making your work life more interesting.
Manage investigator sites and monitor activities for clinical studies throughout the whole trial lifecycle.
Build and maintain good relationships with site staff to ensure deadlines and deliverables are met
You will have complete ownership of the sites you are assigned to, from study start-up to close-out
Hold a degree in life sciences or a license as a healthcare professional
Experience in managing investigator sites
3 years (ideally) monitoring experience, within a Pharma company or CRO
In-depth knowledge of ICH-GCP guidelines and local and international regulations
Fluent in Dutch and English
Good work-life balance
If this job appeals to you please apply here or on the NonStop Consulting website or send it to me, Maria Lynch, on my Linkedin. If you are not available but you know someone that would be interested , please forward this to them and help the people in your network.
NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.