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)
🏢 Altro
📍 Italia