Overview
In this role you drive the design, execution and oversight of global, mostly low-complexity clinical studies. You will work closely with cross-functional teams to meet study deliverables while upholding scientific and operational excellence. The position centers on oncology/hematology-focused research and early development, offering opportunities to influence protocol development, risk management and data-driven decision making. This is a chance to impact patient care through rigorous trial management and collaboration.
Verantwortungsbereiche
- Lead or support development of clinical protocols, amendments and related study documents with the Medical Lead and teams
- Provide medical and scientific input for study processes and regulatory documents
- Contribute to study concept feasibility and operational execution plans
- Collaborate with cross-functional teams to select high-performing sites to meet recruitment goals
- Lead or support global cross-functional Clinical Trial Teams to ensure timely delivery of objectives
- Conduct ongoing medical-scientific reviews of trial data, including safety trend analysis and data interpretation
- Prepare and lead dose escalation meetings and coordinate real-time access to trial data
- Proactively manage risk mitigation and implementation strategies at the trial level
- Forecast and manage study budgets with stakeholders
- Set vendor strategies and timelines for assigned studies
- Implement best practices for trial management and share lessons learned
- Represent the group in cross-functional initiatives and act as a Subject Matter Expert
Zentrale Anforderungen
- Degree in life sciences or healthcare
- Strong understanding of clinical trial methodology, especially in early development
- Experience in clinical trials or development with ability to manage multiple studies
- Proficiency in operational project management (planning, prioritization, problem-solving)
- Strong interpersonal and leadership skills
- High learning agility and adaptability
- Familiarity with ICH-GCP guidelines and clinical finance principles
- Excellent written and verbal English communication
- Commitment to diversity, inclusion and ethical practices
- Oncology/hematology knowledge is highly desirable
- leadership
- cross-functional collaboration
- problem-solving
- clinical trial methodology
- early clinical development
- regulatory document input
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