Medical Science Liaison

Advanced Clinical; Lérida; A distancia; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A leading biopharmaceutical firm is seeking an experienced Clinical Trial Educator to support clinical development programs across Europe. This remote position offers the opportunity to work closely with key investigators and enhance trial delivery. The ideal candidate has 5–10 years of experience in clinical research, a strong understanding of clinical development processes, and excellent communication skills. Join a collaborative environment focused on innovation and patient outcomes.

Servicios

Opportunity to make a meaningful impact on global clinical programs

Collaborative, science-driven environment

Cross-functional exposure

Formación

• 5–10 years of experience in clinical research, ideally as a Clinical Trial Educator or similar role.
• Strong understanding of clinical development processes and ICH-GCP guidelines.
• Fluent in English; additional European languages are an asset.

Responsabilidades

• Build and maintain strong partnerships with investigators and site staff.
• Deliver scientific and clinical education on the investigational compound.
• Support study start-up and ongoing trial execution.

Conocimientos

Clinical Research

Communication

Autonomy

Educación

Degree in Life Sciences, Pharmacy, Nursing, or related discipline

Descripción del empleo

Clinical Trial Educator – Europe

Location: Remote, Europe

Industry: Biopharmaceutical / Clinical Development

Therapy Area: Rare disease

About the Role

We are seeking an experienced Clinical Trial Educator (CTE) to support clinical development programs across Europe. This position offers the opportunity to work directly with leading investigators and study sites, helping to ensure excellence in clinical trial delivery.

The CTE will serve as a key scientific resource and educational partner, strengthening site engagement, facilitating understanding of protocols, and supporting high-quality trial conduct aligned with sponsor objectives and Good Clinical Practice (GCP).

Key Responsibilities

• Build and maintain strong partnerships with investigators, site staff, and key opinion leaders to enhance engagement and study performance.
• Deliver scientific and clinical education on the investigational compound, protocol requirements, and disease area.
• Support study start-up and ongoing trial execution through site training, troubleshooting, and proactive communication.
• Gather insights from the clinical field to inform development strategies and improve operational efficiency.
• Collaborate closely with internal cross‑functional teams, including Clinical Operations, Medical Affairs, and Clinical Development.
• Ensure all interactions adhere to ethical, regulatory, and company compliance standards.

Qualifications & Experience

• Degree in Life Sciences, Pharmacy, Nursing, or related discipline (advanced degree preferred).
• 5–10 years of experience in clinical research, ideally as a Clinical Trial Educator, MSL, or similar site‑facing role within a sponsor environment.
• Strong understanding of clinical development processes and ICH‑GCP guidelines.
• Proven ability to communicate complex scientific information credibly and clearly.
• Fluent in English; additional European languages are an asset.
• Comfortable working autonomously across multiple countries and therapeutic areas.

What We Offer

• The opportunity to make a meaningful impact on global clinical programs.
• A collaborative, science‑driven environment focused on innovation and patient outcomes.
• Cross‑functional exposure within a leading sponsor organisation.