Clinical Trial Site Liaison

Apsida Life Science; Verona; Remote; EUR 42,000 - 64,000; Full time

Job summary

Apsida Life Science è alla ricerca di un Clinical Trial Site Liaison esperto per supportare attività di ricerca clinica in tutta l'Italia. Questo ruolo operativo si concentra sulla costruzione di relazioni con investigatori e siti di sperimentazione, supportando la delivery dello studio e collaborando con i team di Clinical Operations e i partner CRO.

I candidati con esperienza in operations cliniche, gestione siti o ruoli di liaison sono invitati a candidarsi.

Qualifications

• Experience as 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.

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

CTSL/CTL experience

Clinical operations experience

Investigator-site liaison experience

GCP knowledge

Cross-functional collaboration

Travel willingness

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.

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.