Senior Clinical Regulatory Manager
Location | Europe |
Discipline: | Regulatory Affairs, Clinical Research |
Job type: | Permanent |
Contact name: | Jolie Trahar |
Contact email: | jolie.trahar@rbwconsulting.com |
Contact phone: | 01293364082 |
Job ref: | JMTSRCM |
Published: | 8 days ago |
Expiry date: | 22 Aug 2025 23:59 |
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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