Clinical Research Associate I​/Clinical Research Associate II

Employer Industry: Clinical Research Organization (CRO)

• Permanent, remote-based position with reasonable travel commitments
• Opportunity for career advancement and growth within the organization
• Supportive and collaborative work environment with a strong focus on work/life balance
• Lower than average number of protocols, allowing for in-depth expertise
• High retention rates and a culture that values employee input and satisfaction

• Monitor and manage the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted in compliance with protocols, SOPs, ICH‑GCP, and applicable regulations
• Coordinate activities for study setup, including investigator identification and regulatory submissions
• Conduct pre‑study and initiation visits to ensure readiness for study implementation
• Identify potential study risks and propose solutions for mitigation

• Life science degree and/or equivalent experience
• At least 6 months of experience as a Clinical Research Associate (CRA) in a CRO or the pharmaceutical/biotech industry
• Experience managing oncology studies
• Availability for domestic travel, including overnight stays, up to approximately 50‑60%
• Fluency in English and Italian

• Experience with study start‑up activities

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We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer.