Impactful Clinical Lead — Rare Diseases & Oncology

Premier Research Group; España; Sur place; EUR 80 000 - 110 000; Plein temps

Résumé du poste

Premier Research is seeking a Clinical Lead II specializing in Rare Diseases and Oncology to join our Clinical Management team. You will help biotech, medtech, and specialty pharma partners transform ideas into medicines, devices, and diagnostics while delivering life-saving outcomes.

The role involves leading site management, performing sponsor communications, and ensuring quality and audit readiness across trials. Onsite monitoring experience in CRO settings is essential.

Qualifications

• Bachelor’s degree or equivalent in clinical/biological/science field.
• 2+ years as Clinical Lead in a CRO with onsite monitoring experience.
• Experience in Rare Diseases and Oncology, including CAR-T or Cell Gene Therapy is a plus.
• Knowledge of clinical financials, budgets, pass-through and resource management.

Responsabilités

• Serves as initial point of contact for site management and monitoring quality concerns (sPIP initiation and oversight).
• Plans, presents and participates in sponsor calls, providing status updates on clinical deliverables.
• Oversees quality of monitoring and site management deliverables via dashboards/reporting tools.
• Monitors clinical operations metrics and timelines; tracks data entry timelines and query aging.
• Ensures audit readiness and supports sites in remediation/responses to audit findings.
• Escalates quality events and other critical issues through established channels.

Formation

Bachelor’s degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field

Description du poste

Premier Research is seeking a Clinical Lead II specializing in Rare Diseases and Oncology to join our Clinical Management team. You will help biotech, medtech, and specialty pharma partners transform ideas into medicines, devices, and diagnostics while delivering life-saving outcomes.

The role involves leading site management, performing sponsor communications, and ensuring quality and audit readiness across trials. Onsite monitoring experience in CRO settings is essential.