Senior Clinical Regulatory Manager

RBW Consulting LLP; Paris; À distance; EUR 70 000 - 100 000; Plein temps

Résumé du poste

An innovative oncology-focused CRO is seeking a Senior Clinical Regulatory Manager to enhance their Regulatory Affairs team. The role is fully remote, offering autonomy and flexibility within an international collaborative environment. Candidates should have over 5 years of Regulatory Affairs experience, direct clinical trial application submission knowledge, and line management experience preferred. Join now and contribute to advancing oncology clinical trials across Europe.

Prestations

Fully remote role

Flexibility and autonomy

Opportunity for career progression

Qualifications

• 5+ years’ experience in Regulatory Affairs within clinical trials.
• Direct experience preparing and submitting CTIS and RIAS clinical trial applications.
• CRO experience preferred; oncology experience is a strong bonus.

Responsabilités

• Support and eventually lead the Regulatory Affairs (RA) function.
• Deputise for the Head of RA.
• Coach, train, and oversee a busy team.

Connaissances

Regulatory Affairs

Clinical Trials

Team Management

Fluent English

Description du poste

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 aSenior Clinical Regulatory Managerto support and eventually lead the Regulatory Affairs (RA) function within a specialist CRO.

You’lldeputise for the Head of RAand play a key role in coaching, training, and overseeing a busy team.

What You’ll Bring:

·5+ years’ experiencein Regulatory Affairs within clinical trials

·Direct experiencepreparing and submittingCTISandRIASclinical trial applications

·CRO experience preferred (but pharma backgrounds welcome)

·Oncology experience is astrong bonus but not essential

·Fluent inwritten and spoken English; additional languages are a plus

·Comfortable in afast-paced environmentwith shifting priorities

·Line management experience is a strongadvantage

What’s on Offer:

·Afully remoterole with flexibility and autonomy

·A collaborative, international team environment

·Clear pathway toteam 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