Clinical Trial Site Liaison

Apsida Life Science; Italia; Teletrabalho; EUR 45 000 - 65 000; Tempo integral

Resumo da oferta

Apsida Life Science is seeking an experienced Clinical Trial Site Liaison to support clinical research activities across Italy. This hands-on contract role focuses on building relationships with investigators and sites, supporting study delivery, and collaborating with Clinical Operations teams and CRO partners.

Candidates with CTSL/CTL, CRA, CTM, or similar backgrounds, strong GCP knowledge, and fluency in Italian are encouraged to apply.

Qualificações

• Experience as CTSL/CTL, CRA, CTM or similar.
• Strong clinical trial and investigator-site experience.
• GCP knowledge and CRO/sponsor liaison experience.
• Fluent Italian and based in Italy.

Responsabilidades

• Build relationships with investigators and clinical research sites.
• Support site engagement, study start-up and ongoing trial delivery.
• Liaise between sponsor, CRO and internal clinical teams.
• Address site needs and ensure GCP-compliant study conduct.

Conhecimentos

CTS/CTL experience

GCP knowledge

Investigator-site relations

Travel willingness

Descrição da oferta de emprego

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.