Oncology Clinical Research Lead — Trials & Coordination

Proclinical Staffing; Basel; Vor Ort; CHF 120.000 - 150.000; Vollzeit

Zusammenfassung

Proclinical is seeking a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, focusing on low-complexity trials. You will collaborate across cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The role requires a strong background in clinical research, particularly in oncology or hematology, with excellent leadership and problem-solving skills.

Qualifikationen

• Degree in life sciences or healthcare; advanced degree preferred.
• Experience in clinical trials; early development; multi-study management.
• Strong knowledge of ICH-GCP and regulatory/clinical finance principles.

Aufgaben

• Lead or support development of clinical protocols and amendments with Medical Lead.
• Provide medical and scientific input for study processes and regulatory documents.
• Contribute to feasibility assessments and operational execution plans.
• Collaborate to select high-performing sites to meet recruitment goals.
• Lead or support global cross-functional Clinical Trial Teams (CTTs).
• Review trial data for safety trends and data interpretation.
• Coordinate dose escalation meetings and real-time data availability.
• Manage risk mitigation and implementation strategies at trial level.
• Forecast and manage study budgets with stakeholders.
• Set vendor strategies and timelines for studies.
• Implement best practices for trial management and share lessons learned.
• Represent the group in cross-functional initiatives as SME.

Kenntnisse

Clinical research

Project management

Leadership

Communication

English proficiency

Ausbildung

Life sciences degree

Advanced degree preferred

Jobbeschreibung

Proclinical is seeking a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, focusing on low-complexity trials. You will collaborate across cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The role requires a strong background in clinical research, particularly in oncology or hematology, with excellent leadership and problem-solving skills.