Immatics
SeniorClinicalOperationsLead
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“Senior Clinical Operations Lead at Immatics. Skills: Clinical Operations, Vendor Management, Stakeholder Management. Ensure GCP-compliant planning and execution of clinical studies. Oversee GCP-compliant monitoring of outsourced activities”
What You'll Achieve.
delivering novel PRAME immunotherapies to patients with cancer; consistently push projects to completion
Industry & Context.
proposing appropriate solutions or mitigation strategies; think pragmatically; clear view of the bigger picture
What They're Looking For.
Must Have
Master’s degree, 6+ years of experience in clinical project management, fluent and clear communication in German and English (at least C1-level)
Nice to Have
preferably in life sciences or a related field, ideally in oncology and cell therapy
What You'll Do.
Ensure GCP-compliant planning and execution of clinical studies
Oversee GCP-compliant monitoring of outsourced activities
Contribute to selection and qualification of vendors
Take responsibility at study level for feasibility assessments
Manage Clinical Operations vendors
Provide operational support to central laboratories
Perform administrative clinical trial tasks
Ensure assignment and completion of study-related training
Develop and maintain SOPs and training materials
Mentor less experienced Clinical Operations Leads
How You'll Work.
Team & Collaboration
work in an interdisciplinary environment; collaboration with internal and external stakeholders; collaboration with the Vendor Governance team; effective collaboration skills
Communication Scope
fluent and clear communication in German and English (at least C1-level)
Process & Methodology
clinical project management, project reviews, risk and issue management, matrix coordination
Full Job Description
**OVERVIEW** We are currently seeking a full- or part-time (min. 32 hrs/ week) **Senior Clinical Operations Lead*** to strengthen our Clinical Trial Leadership team. You will work in Tübingen, Munich or remote within Germany in an interdisciplinary environment with colleagues from Germany and the US and will contribute to our mission of delivering novel PRAME immunotherapies to patients with cancer. **YOUR MISSION** Your main responsibilities will include but are not limited to the following tasks: * Ensure and support GCP-compliant planning and execution of clinical studies within Clinical Operations, including provision of study cost information and regular updates impacting global timelines and budgets * Oversee GCP-compliant monitoring of outsourced Clinical Operations activities, conduct regular meetings, and escalate issues as needed * Contribute to the selection and qualification of GCP/GCLP vendors within clinical outsourcing, and take responsibility at study level for feasibility assessments, site selection, risk and issue management, matrix coordination, and collaboration with internal and external stakeholders * Lead project reviews, manage processes, and escalate key issues, proposing appropriate solutions or mitigation strategies * Manage Clinical Operations vendors and support the Vendor Governance team through feedback and collaboration * Provide operational support to central laboratories * Perform administrative clinical trial tasks (finance, logistics, and communication), ensure assignment and completion of study-related training, develop and maintain SOPs and training materials, and mentor less experienced Clinical Operations Leads upon request **YOUR PROFILE** You hold at least a Master’s degree, preferably in life sciences or a related field, and bring 6+ years of experience in clinical project management within the pharmaceutical or biotech industry, ideally in oncology and cell therapy. You feel comfortable in a matrix environment and are pass
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