Job Description

About Latium

Latium Research is a seed-stage biotech spun out of the Universities of Strathclyde & Manchester; Our non-viral gene-delivery platform has selectively eliminated glioblastoma (GBM) cells in pre-clinical models, and we are now assembling the data package for a first-in-human Phase I trial.

The opportunity

Reporting to the founders, you will be the operational engine that drives our GBM programme from final GLP tox through first-patient-in. You will co-ordinate academics, CROs, manufacturing, vendors and regulators so the science team can stay focused on discovery.

Key responsibilities

1. Project leadership to build and maintain the integrated project plan (timeline, budget, risk log) for GLP tox, CMC, regulatory and clinical work-streams.

2. Regulatory operations - compile and submit CTA/IND, ethics track RFIs, manage agency correspondence (MHRA, FDA, EMA).

3. Vendor & CRO management - source, contract, kick-off and oversee CROs and specialist labs; track KPIs and invoices.

4. Study start-up - support protocol development, investigator brochure, site selection and green-light packages.

5. Data & documentation - own the TMF/eTMF, deviation log and CAPA actions to inspection-ready standards.

6. Stakeholder communication - prepare dashboards and board packs; chair weekly cross-functional calls.

Ideal profile

1. 3-5 yrs experience coordinating or managing Phase I/II trials (CRO, biotech or NHS R&D office).

2. Hands-on contributor to ? 1 CTA or IND submission.

3. STEM BSc (or higher) with working knowledge of oncology or gene-therapy terminology.

4. Comfortable juggling multiple vendors and shifting priorities in a start-up setting.

5. Prince2/PMP or ACRP/SoCRA certification (nice-to-have).

Why Latium?

1. Impact: bring a first-in-class therapy to patients with < 10 % five-year survival.

2. Growth: direct exposure to founders, KOLs and investors from day one.

How to apply

Click "Apply" on Indeed and upload your CV. Please add a short cover note describing your early-phase oncology or gene-therapy experience. We review applications weekly and aim to respond within seven days.

Job Type: Full-time

Pay: 40,000.00-50,000.00 per year

Benefits:

On-site gym On-site parking
Schedule:

Monday to Friday No weekends
Work Location: In person

Reference ID: LatResGMB0707
Expected start date: 01/09/2026