Clinical Trial Site Liaison
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Experience as a CTSL/CTL, CRA, CTM, Clinical Project Manager or similar.
Strong clinical trial and investigator-site experience.
MSL experience considered, ideally alongside clinical trial exposure.
GCP knowledge and experience working with investigators, sites and CROs.
Experience with autoimmune, neurology or neuroscience backgrounds.
Fluent Italian and based in Italy.
Professional Traits & Work Ethic Strong communication and relationship-building skills.
Proactive, organised and reliable, with a service-oriented approach.
Comfortable working independently within an international team.
Willing to travel nationally across Italy.
Role Responsibilities Build relationships with investigators and clinical research sites.
Support site engagement, study start-up and ongoing trial delivery.
Liaise between the sponsor, CRO and internal clinical teams.
Address site needs and support GCP-compliant study conduct.
Contract: Initial 12 months, with potential extension.
Commitment: Full-time preferred; 0.5–0.8 FTE considered.
Location: Home-based in Italy, with national travel occasionally.
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