Clinical Operations Project Manager

Experteer Overview  In this role you oversee the operational delivery of regional clinical studies, ensuring timelines, quality, and regulatory compliance. You work closely with sponsor teams, CRAs, and cross‑functional partners to drive study execution in Italy and Greece. You will combine hands‑on site‑facing oversight with proactive risk management to support timely drug development. This position offers opportunities to shape operational delivery within a global CRO/FSP model and to lead cross‑functional collaboration from a Rome base.
Retribuzione / Benefits   Execute and monitor clinical trials within Italy and Greece ensuring delivery on time, budget, and quality
Provide functional oversight to CRAs and supervise their study‑level training
Support site engagement through visits and audits as needed
Review monitoring visit reports, CAPA implementation, and ensure protocol adherence
Assist with inspection readiness and manage study risk, issues, and contingencies
Coordinate cross‑functional activities to achieve milestones and address study issues
Develop and maintain study plans/timelines and organize regular follow‑up meetings
Responsabilità   Bachelor’s degree in Life Sciences or related field
3+ years as Project Manager and 5+ years in clinical research
Strong knowledge of ICH‑GCP and regulatory requirements
Experience in Early Phase – Phase I/II trials
Oncology therapeutic area knowledge (advantage)
Proven… etc
Strong communication and stakeholder management skills
Ability to manage multiple priorities in a matrix environment
Excellent English
Strong operational leadership and risk management skills
Collaborative cross‑geography teamwork
Willingness to work at sponsor's office in Rome ≥3 days/week
Requisiti fondamentali   incentive plans
bonuses
health and welfare benefits
potential for career growth
remote/onsite flexibility
Rome-based work arrangement

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