22 ott - Milano
Apsida Life Science
We're partnering with a clinical-stage biopharmaceutical company seeking an experienced Clinical Trial Site Liaison to support clinical research activities across Italy. This is a hands-on contract role focused on building relationships with investigators and clinical trial sites, supporting study delivery, and working closely with Clinical Operations teams and CRO partners. Candidates with a background in clinical operations, site management or clinical trial liaison roles are encouraged to connect.
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. Comfortable working independently within an international team.
Role Responsibilities
Build relationships with investigators and clinical research sites. 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; Location: Home-based in Italy, with national travel occasionally.
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