Jobtyp: Freelance

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Jobinhalt

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.
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Frist: 31-12-2025

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