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Senior clinical regulatory manager

Warrington
Jr United Kingdom
Manager
Posted: 24 August
Offer description

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Senior Clinical Regulatory Manager, warrington, cheshire

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Client:

RBW Consulting


Location:


Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2


Posted:

22.08.2025


Expiry Date:

06.10.2025

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Job Description:

Senior Clinical Regulatory Manager

Location: Fully Remote (Based out of UK, France, Italy, Spain, Sweden or Republic of Ireland)

Travel: Occasional travel to conferences (a few times per year)

Start Date: ASAP

Team Expansion Role – Pathway to Full Team Management

Are you a hands-on Regulatory Affairs professional with a passion for clinical trials and a drive to grow into leadership? Join a dynamic, fast-paced SME-sized CRO specialising in oncology, where your expertise will shape the future of our expanding Regulatory Affairs team.

About the Role:

Due to increasing workload and strategic growth, we’re hiring a Senior Clinical Regulatory Manager to support and eventually lead the Regulatory Affairs (RA) function within a specialist CRO.

You’ll deputise for the Head of RA and play a key role in coaching, training, and overseeing a busy team.

? What You’ll Bring:

* 5+ years’ experience in Regulatory Affairs within clinical trials
* Direct experience preparing and submitting CTIS and RIAS clinical trial applications
* CRO experience preferred (but pharma backgrounds welcome)
* Oncology experience is a strong bonus but not essential
* Fluent in written and spoken English; additional languages are a plus
* Comfortable in a fast-paced environment with shifting priorities
* Line management experience is a strong advantage

What’s on Offer:

* A fully remote role with flexibility and autonomy
* A collaborative, international team environment
* Clear pathway to team management
* Opportunity to shape regulatory strategy in a growing oncology-focused CRO

Ready to take the next step in your regulatory career?

Apply now and help drive innovation in oncology clinical trials across Europe.

Key Words:

Clinical trial, study, studies, trials research, GCP, regulatory affairs, RA, oncology, cancer, ICF, CTIS, RIAS, submission, authoring, writing, application, preparation, management, manager, supervisor, team leader, supervision, coaching, training

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