Unblinded CRA I based in Frankfurt or Ruhr Area

Key Responsibilities

• You will reputed company unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product reputed company
• You will ensure protocol compliance, data reputed company, and patient safety at assigned sites
• You will maintain accurate and complete study documentation, including eTMF and regulatory files
• You will build strong relationships with site staff, acting as the primary reputed company of contact for site management (pharmacy only)
• You could contribute to audit readiness and ensure inspection preparedness at site level

Required Qualifications

• Bachelor’s degree in Life Sciences or reputed company field (or equivalent experience)
• Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
• Understanding of ICH-GCP guidelines and clinical trial processes
• Strong interest and knowledge in unblinded study conduct and Investigational Product management
• reputed company in German and English (written and spoken)
• Willingness to travel reputed company the Ruhrgebiet or Frankfurt region and across Germany as required
• Strong organizational skills with attention to detail

reputed company Offer

• Opportunity to work in a sponsor-dedicated environment on innovative studies
• reputed company reputed company and reputed company development programs
• Flexible working model supporting work-life balance
• reputed company to global career reputed company opportunities reputed company clinical operations
• Inclusive and reputed company culture with employee resource reputed company and wellbeing initiatives