Biotech Project Manager – Oncology

2 weeks ago

Galway, Galway, Ireland BioTalent Full time

Role: Biotech Project Manager – Oncology (CMC/Clinical Support)

Location: Galway, IE

The Company

A pioneering cell therapy biotech is on a mission to transform the treatment of solid tumours through a unique allogeneic neutrophil-based therapy platform. Unlike patient-specific T-cell therapies, this approach is donor-derived, scalable, and consistent, enabling it to be manufactured at scale and delivered to patients more efficiently. The therapy harnesses the natural tumour-infiltrating and tumour-killing abilities of neutrophils, which can also be engineered to enhance their anti-cancer activity. This makes the platform a powerful, differentiated strategy designed to overcome tumour resistance and improve patient outcomes.

The company is entering an exciting growth phase, with its first-in-human clinical trial scheduled to begin in Galway within the next 12 months. To support this, the biotech has partnered with a CDMO to handle GMP manufacturing, while the UK headquarters drive innovation, translational research, and CMC strategy. With strong leadership, a visionary scientific platform, and a clear clinical path ahead, this is an exceptional opportunity to contribute to a next-generation oncology therapy at the point where science is translating into patient impact.

The Team

This role reports directly to the CSO.

The Opportunity

This is a newly created position to support the upcoming tech transfer and clinical trial readiness in Galway. The Project Manager will play a central role in coordinating stakeholders, ensuring regulatory and operational compliance, and managing timelines for this high-impact oncology programme.

Responsibilities


• Manage timelines for trial readiness in Galway


• Liaise with CDMO partner and CSO


• Support compliance and documentation requirements


• Drive cross-functional coordination with CSO, CDMO, and internal teams


• Provide progress reporting to leadership (CSO and Chief Development & Regulatory Officer)

Requirements


• Proven project management experience in a regulated life sciences setting, ideally with CMC exposure


• Strong organisational and stakeholder management skills


• Experience leading cross-functional projects with CDMOs, CSOs, and regulatory stakeholders


• Based in, or willing to relocate to, Galway and able to work primarily on-site

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