Unblinded Clinical Research Associate (German-speaking)

About the role

ICON is a global healthcare intelligence and clinical research organisation. As a CRA II, you will design and analyse clinical trials, interpret complex medical data and help advance new treatments. The role is open to CRAs with fluent German who are willing to travel abroad to carry out monitoring activities, also in Germany.

Key responsibilities

• Contribute to clinical trial monitoring, taking responsibility for your deliverables and working collaboratively
• Carry out site qualification, initiation, monitoring and close-out visits
• Ensure protocol compliance, data integrity and patient safety
• Work with investigators and site staff to run studies smoothly
• Review data and resolve queries
• Help prepare and review study documentation, including protocols and clinical study reports

Required profile

• Bachelor's degree in a scientific or healthcare-related field
• At least 2 years of experience as a Clinical Research Associate
• Fluent German (mandatory)
• Willingness to travel, approximately 60%
• Legal right to work in the country where the role is based

Required skills

• In-depth knowledge of clinical trial processes, regulations and ICH-GCP guidelines
• Strong organisational and communication skills with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment

What we offer

• Competitive base salary and performance-related incentives
• Health and wellbeing programmes, including medical, dental and vision coverage where applicable
• Retirement and pension plans, life assurance and disability coverage
• Employee assistance programmes and learning and development opportunities