Experteer Overview In this role you lead the medical and clinical aspects of all phases in the drug development process, driving strategy, study design, and regulatory alignment. You will act as a clinical/medical representative in meetings with external partners and authorities, shaping protocols and study documents. You guide safety monitoring, data interpretation, and regulatory submissions, working with cross‐functional teams to advance therapeutic programs. This role offers impact across clinical development, collaboration with academic centers, and leadership opportunities within a mission‐driven global organization.



Retribuzione / Benefits Provide medical content and leadership for clinical studies Serve as therapeutic lead and oversee medical monitoring Design and approve scientific methods underlying protocols Ensure subject safety and timely adverse event reviews Collaborate with trial teams and safety committees as needed Contribute to and approve study protocols, IBs, CSRs, ICFs, and CRFs Interpret and document clinical data for regulatory submissions and publications Collaborate with leading academic medical centers Recruit, guide and motivate clinical investigators Ensure study compliance with SOPs and GCPs Participate in long‐range strategic planning Line management responsibilities Responsabilità MD degree with minimum 5 years of clinical drug development experience Drug development experience in Rheumatology Knowledge of regulatory submissions Excellent written and verbal communication skills Ability to travel Demonstrated expertise in clinical trial design, conduct and data interpretation Vigilant proactive problem solving Strong leadership abilities #J-18808-Ljbffr

📌 Senior/ executive medical director (Italia)
🏢 Experteer Italy
📍 Italia