Field MSL - Hematology/Oncology (Italy & Germany)

Quetzal; Italia; À distance; EUR 80 000 - 110 000; Temps partiel

Résumé du poste

Quetzal Therapeutics seeks an experienced Medical Science Liaison (MSL) to support a multinational Phase 3 haematology/oncology trial across Italy and Germany. This field-based role engages investigators and treatment centres, driving trial awareness and high-quality scientific exchange within compliance.

The candidate will work independently in a distributed territory, acting as a key scientific interface with external stakeholders while navigating regulatory requirements and pharmacovigilance

Qualifications

• Advanced scientific or healthcare degree required.
• Experience as a field-based MSL in oncology or haematology.
• Ability to work independently across a multi-site territory.
• Experience with GCP, pharmacovigilance and compliance frameworks.

Responsabilités

• Develop and maintain scientific relationships with investigators and healthcare professionals.
• Support scientific engagement around a Phase 3 haematology trial.
• Deliver high-quality, non-promotional scientific exchange in compliance with regulations.
• Support trial awareness and operational engagement in assigned territories.
• Identify field insights including recruitment challenges and treatment landscape developments.
• Support congress activities, investigator meetings and scientific discussions.
• Document activities and report adverse events per pharmacovigilance requirements.
• Collaborate cross-functionally with Medical Affairs, Clinical Operations and others.

Connaissances

Scientific communication

Independent working

Stakeholder engagement

GCP/compliance knowledge

Multisite territory management

Italian language

Formation

Advanced scientific or healthcare degree (PharmD/PhD/MD/MSc)

Description du poste

Quetzal Therapeutics seeks an experienced Medical Science Liaison (MSL) to support a multinational Phase 3 haematology/oncology trial across Italy and Germany. This field-based role engages investigators and treatment centres, driving trial awareness and high-quality scientific exchange within compliance.

The candidate will work independently in a distributed territory, acting as a key scientific interface with external stakeholders while navigating regulatory requirements and pharmacovigilance