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Director of Research

SRG
Posted a day ago, valid for 18 days
Location

Altrincham, Cheshire WA141BL, England

Salary

£48,000 - £57,600 per year

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Contract type

Full Time

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Sonic Summary

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  • SRG is seeking a Director of Research for a seed-stage biotech in Cheshire focused on a non-viral gene-delivery platform for glioblastoma.
  • The role requires a PhD or equivalent in a related discipline and significant experience managing Phase I/II trials, with a salary of £80,000 to £100,000.
  • Key responsibilities include project leadership, regulatory operations, vendor and CRO management, and stakeholder communication.
  • The ideal candidate should have proven experience with CTA or IND submissions and familiarity with GxP, ICH, and MHRA processes.
  • This position offers an opportunity to make a significant impact in oncology and be part of a passionate team driving innovative science into the clinic.

Director of Research

Permanent

Cheshire

SRG is delighted to be working with a seed-stage biotech to help them find a Director of Research. The organisation is developing a non-viral gene-delivery platform targeting glioblastoma cells and has shown incredibly positive results in pre-clinical models.

Reporting directly to the founders as the Director of Research you will be the operational engine that drives the platform from final GLP tox through first-patient-in. You will co-ordinate academics, CROs, manufacturing, vendors and regulators to drive this exciting project into clinic.

Key responsibilities

  • Project leadership to build and maintain the integrated project plan (timeline, budget, risk log) for GLP tox, CMC, regulatory and clinical work-streams.
  • Regulatory operations - compile and submit CTA/IND, ethics track RFIs, manage agency correspondence (MHRA, FDA, EMA).
  • Vendor & CRO management - source, contract, kick-off and oversee CROs and specialist labs; track KPIs and invoices.
  • Study start-up - support protocol development, investigator brochure, site selection and green-light packages.
  • Stakeholder communication - prepare dashboards and board packs; chair weekly cross-functional calls.

Ideal profile

  • PhD (or equivalent) in a related discipline with working knowledge of oncology or gene-therapy terminology.
  • Significant experience coordinating or managing Phase I/II trials in a CRO, biotech or pharma.
  • Proven experience with CTA or IND submission and tracking.
  • Experience with liposomes or lipid nanoparticles would be advantageous.
  • Familiar with GxP, ICH, and MHRA processes.
  • Strong communication and vendor management skills

Are you ready to shape the future of gene therapy and make a real impact in oncology?

Join a passionate team at the forefront of biotech innovation, where your expertise will drive breakthrough science into the clinic. If you thrive in dynamic environments and want to be part of something truly transformative, we want to hear from you!

Apply now by attaching your CV in Word, or contact Paige Keenan () or Nathan Fairhurst () for further information about this new role.

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.