Clinical Trial Site Liaison

Apsida Life Science; Italia; Remote; EUR 45,000 - 65,000; Full time

Job summary

Apsida Life Science is partnering with a clinical-stage biopharmaceutical company to recruit an experienced Clinical Trial Site Liaison to support activities across Italy. This hands-on contract role focuses on building relationships with investigators and clinical trial sites, and coordinating with Clinical Operations teams and CRO partners.

Based in Italy, you will travel nationally to sites, support study start-up and ongoing trial delivery, and ensure GCP-compliant conduct.

Qualifications

• Experience as CTSL/CTL, CRA, CTM, Clinical Project Manager or similar.
• Strong clinical trial and investigator-site experience.
• GCP knowledge and experience working with investigators, sites and CROs.
• Experience with autoimmune, neurology or neuroscience backgrounds.
• Fluent Italian and based in Italy.

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.

Skills

Communication

Relationship-building

Project management

Independent working

Travel readiness

Job description

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.
• 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.