Clinical Trial Site Liaison
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.
Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.
- 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. xlwpduy
Location: Home-based in Italy, with national travel occasionally.
Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.
- 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. xlwpduy
Location: Home-based in Italy, with national travel occasionally.