Team Lead, Site Operations

_ Join Immaticsandshape thefuture ofcancerimmunotherapy; one patient at atime! _

Immaticsis committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME , a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCRbispecifics.

• Innovative Environment: Helptopioneeradvancementsincancer immunotherapy.

• Collaborative Culture: Be part ofa diverse team dedicated to yourprofessionalgrowth.

• Global Impact: Contribute to therapiesthatmakealastingimpactonpatientsglobally.

The Team Lead, Site Operations is the formal people leader and functional process owner for assigned Site Operations personnel within Clinical Operations. The role is accountable for line management, resource planning, capability development, functional quality, and the design, maintenance, and continuous improvement of designated Site Operations and Clinical Operations processes. The Team Lead enables consistent, compliant execution across Germany and the United States and partners closely with Clinical Operations Leads to ensure appropriately skilled resources are assigned to studies.

Reports to: Vice President, Clinical Operations

Location: Remote

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline required.

• 8 to 10 years of experience in Clinical Operations or related functions within biotech or pharmaceutical industries, with 4 to 5+ years of that experience in direct people leadership, managing clinical operations professionals

• Master’sdegree in Life Sciences, Pharmacy, Nursing, or a related discipline

• 5+ years of clinical monitoring experience within the pharmaceutical or biotechnology industry, including roles as a Clinical Research Associate and/or Clinical Trial Manager.

• Demonstrated late phase experience in oncology.

• Experience in cell therapy or other complex investigational therapies strongly preferred.

• Strong working knowledge of ICH-GCP, FDA regulations, and global clinical trial requirements.

• Demonstrated ability to lead cross-functional initiatives and influence stakeholders across multiple organizational levels.

• Proven experience managing resources, priorities, and competing business demands in a dynamic environment.

• History of driving operational improvements and implementing innovative approaches within Clinical Operations.

• Experience supporting regulatory inspections and audit readiness activities.

• Serve as the formal line manager for assigned Site Operations personnel, including Clinical Trial Associates, Clinical Research Associates and Clinical Trial Managers, and other roles as assigned.

• Recruit, onboard, coach, develop, and retain team members who meet role requirements and contribute to a high-performing, collaborative Clinical Operations culture.

• Set individual objectives, provide regular and meaningful performance feedback, conduct formal performance evaluations, and support career development, succession planning, and promotion readiness.

• Create an environment of trust, accountability, inclusion, and psychological safety while addressing performance or conduct concerns promptly and appropriately.

• Ensure team members maintain the training, qualifications, competencies, and functional knowledge required for their assigned responsibilities.

• Partner with the Clinical Operations Leads (COLs) to ensure study roles, priorities, timelines and deliverables are clear, serving as a point of escalation and receive study-performance feedback on team…