Freelance CRA - Risk-based Monitoring

Can you picture yourself in a niche, non-profit CRO with excellent work-life balance? This company uses risk-based monitoring so that you will have a reduced level of site visits and therefore better work-life balance. They also have a much lower manager-employee ratio, so you will receive award-winning support.

Responsibilities:

• Carry out pre-study, initiation, monitoring and close-out site visits
• Ensure compliance with FDA, ICH-GCP and local regulations
• Make sure that regulatory documents are complete and collected
• Carry out data verification of source documents
• Assist with budget negotiation
• Participate in data validation and resolving queries;
• Train and help junior team members to develop.

Qualifications:

• 2years monitoring experience in oncology
• Extensive oncology knowledge
• Possess a science-related Bachelor's degree
• Knowledge ofICH-GCPs
• Clinical trial information systems experience
• Fluency in English is required, fluency in French and Dutch is preferred

Benefits:

• Good salary rates
• Excellent work-life balance (work from home and less site visits
• Award-winning managerial support

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.