Senior Clinical Research Associate I

Job Title: Senior Clinical Research Associate I Job Location: Greece - Remote Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Why This Role Matters Are you ready to take your monitoring expertise to the next level and mentor the next generation of clinical research professionals? As a Senior Clinical Research Associate I (SCRA I), you will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability and operational judgment. In addition to driving patient safety and trial quality, you will serve as a Subject Matter Expert (SME), contribute to regional process improvements, and partner directly with Site Care Partners (SCPs) on early-phase activation activities. Your deep therapeutic insight and leadership will directly safeguard trial integrity, strengthen crucial investigator relationships, and enhance Pfizer's scientific credibility with global external stakeholders. The Impact You Will Make In this senior-level role, you will take on expanded operational and mentorship responsibilities: Advanced Monitoring & Site Management: Independently manage and monitor assigned investigator sites from initiation to database lock. Ensure compliance with Study Monitoring Plans, SOPs, GCP guidelines, and prevailing laws. Site Activation & Preparation: Partner with Site Care Partners prior to site activation on crucial feasibility and site selection processes, Pre-Trial Assessments (PTAs), site activation checklists, Informed Consent Document (ICD) finalization, and Site Initiation Visits (SIVs). Leadership & Mentorship: Actively mentor and train Clinical Research Associates (CRAs) as assigned, supporting their development and operational capability. Subject Matter Expertise: Serve as a Subject Matter Expert (SME) for CRA-related processes and participate in regional or local working groups and process improvement initiatives. Issue Resolution & Compliance: Identify, resolve, and mana