Director of Regulatory Affairs

Company: Kelaca

  • Location: London, United Kingdom
  • Work mode: Hybrid
  • Seniority: Director
  • Employment type: Full-time
  • Posted: Yesterday
  • Offer language: English

Job description

Regulatory Affairs Director

London (hybrid, 3 to 4 days in the office)

£120,000 to £150,000 + benefits

I’m working on a confidential leadership hire for an established early phase CRO in London. Their work centres on first-in-human and early clinical studies for biotech and pharma sponsors, across a broad range of modalities.

This is a regulatory leadership role for a medically qualified professional with hands-on experience of clinical trial applications for medicinal products, from the regulator side as a medical or clinical assessor.

What you’ll do

  • Advise sponsors on the regulatory route into the clinic, including CTA and IND strategy, IMPD and IB content, and scientific advice
  • Act as the lead contact for regulators on behalf of the business
  • Lead a team covering regulatory, scientific writing and drug safety
  • Join sponsor and new business conversations as the senior regulatory voice

What you need

  • Medical degree and GMC registration
  • Experience as a medical or clinical assessor at the MHRA or an equivalent agency
  • Direct experience assessing, authoring or leading CTAs or INDs for medicinal products
  • 8+ years in drug development across a regulator and pharma, a CRO or a regulatory consultancy
  • Experience line managing a team
  • A solid grasp of early phase trial design

You’ll lead the drug safety team, but deep pharmacovigilance systems expertise isn’t required, as there’s an established safety function in place.

Please note this role requires regulatory experience with medicinal products. Experience limited to medical devices, IVDs, CQC or clinical governance won’t be sufficient.

Why consider it

A senior role where regulatory judgement shapes programmes from the very start, with a team to lead and a seat in conversations with sponsors.

Conversations are fully confidential and the client is shared after an initial call. Message me directly or apply here.

Courses that can help you get this job

Similar offers

  • Regulatory Affairs Manager

    Est. €3,740–6,560 / month

    Company: Verbatim Pharma

    Offer language: English Posted:Yesterday
    • Location: United Kingdom
    • Work mode: Hybrid
    • Seniority: Senior
    • Employment type: Full-time
  • Company: Blackfield Associates

    Offer language: English Posted:Yesterday
    • Location: Hampshire, United Kingdom
    • Seniority: Mid level
    • Employment type: Full-time
  • Regulatory Affairs Manager

    Est. €3,740–6,560 / month

    Company: NX Health Limited

    Offer language: English Posted:Yesterday
    • Location: Manchester, United Kingdom
    • Work mode: Hybrid
    • Seniority: Senior
    • Employment type: Full-time
  • Regulatory Affairs Manager

    Undisclosed salary

    Company: Alfa AI

    Offer language: English Posted:3 days ago
    • Location: Bristol, United Kingdom
    • Work mode: Hybrid
    • Seniority: Senior
    • Employment type: Full-time

Get Started. It's FREE

Fill out the form to get started today for FREE: Access all features and preview up to 5 courses of your choice for 2 weeks!

Register

Get started today for FREE: Access all features and preview up to 5 courses of your choice for 2 weeks!

A password will be sent to your email address.

By requesting free demo, you confirm that you have read and understood the privacy policy and you agree to receive marketing communications from AIDIFY regarding product updates, offers, and insights. You can unsubscribe at any time.