03 ago - Roma
Experteer Italy
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 #J-18808-Ljbffr
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PENTA FORMAZIONE
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Adecco Italia