Clinical Research Associate

Senior CRA

Key Responsibilities

• Act as the primary contact for assigned clinical study sites in Germany.
• Conduct PSV, SIV, IMV, and COV visits, ensuring quality and compliance with the Monitoring Plan, SOPs, ICH- GCP, and applicable regulations.
• Support study start-up, including feasibility, site selection, and site initiation activities.
• Manage essential and regulatory documentation and ensure timely completion.
• Support investigator, client, and project team meetings and training.
• Develop site-level patient enrollm...
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