Clinical Trial Liaison

Hlx Life Sciences; Île-de-France; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

Hlx Life Sciences is seeking a Contract Clinical Trial Liaison to support a rare disease programme across Spain, France and the UK. This full-time role collaborates with clinical sites, investigators, KOLs, CROs and internal cross-functional teams to enable study delivery and scientific engagement.

You will build strong relationships, support trial execution, facilitate communication between sites and partners, and address site needs in a fast-paced clinical-stage biotechnology environment.

Qualifications

• Experience in the rare disease therapeutic area.
• Proven experience in clinical trials, clinical operations or medical affairs.
• Experience engaging with clinical sites, investigators and KOLs.
• Excellent communication and stakeholder management skills.
• Ability to work independently and collaboratively in a biotech environment.
• Available for full-time (1 FTE) contract.

Responsibilities

• Build and maintain relationships with clinical sites, investigators and KOLs across Europe (Spain, France and the UK).
• Support clinical trial execution and study delivery.
• Facilitate communication between sites, CROs and internal teams.
• Support scientific engagement and address site-related needs.
• Identify and resolve site challenges to support study progress.
• Operate in a fast-paced clinical-stage biotech environment.

Skills

Rare disease experience

Clinical trials experience

Stakeholder management

Communication skills

Independent work

Full-time availability

Job description

Job Description: Contract Clinical Trial Liaison – Rare Disease

Location: Europe – Spain, France and the UK

Contract: Full-time (1 FTE), Contract

Therapeutic Area: Rare Diseases

About the Role

We are supporting a clinical-stage biotechnology company seeking an experienced Contract Clinical Trial Liaison to support an ongoing clinical programme within the rare disease space across Spain, France and the UK.

This role will work closely with clinical sites, investigators, key opinion leaders (KOLs), CROs and internal cross-functional teams to support effective clinical study delivery and scientific engagement.

Key Responsibilities

• Build and maintain strong relationships with clinical sites, investigators and KOLs across Spain, France and the UK.
• Support clinical trial execution and effective study delivery.
• Facilitate communication and collaboration between sites, CROs and internal teams.
• Support scientific engagement and address site-related needs throughout the clinical programme.
• Help identify and resolve site challenges to support study progress.
• Operate effectively in a fast-paced, clinical-stage biotech environment.

Key Requirements

• Essential: Previous experience within the rare disease therapeutic area.
• Strong experience in clinical trials, clinical operations or medical affairs.
• Proven experience engaging with clinical sites, investigators and KOLs.
• Excellent communication, relationship-building and stakeholder management skills.
• Ability to work independently and collaboratively in a dynamic biotech environment.
• Availability to commit to a full‑time (1 FTE) contract.

Contract Overview

This is an opportunity to support an ongoing rare disease clinical programme within a clinical-stage biotechnology company, working across multiple European markets and engaging with key clinical stakeholders.