Associate Director, Regulatory Affairs - UK & Ireland

BeiGene, Ltd.; United Kingdom; Remote; GBP 81,000 - 101,000; Full time

Job summary

BeOne is seeking an Associate Director of Regulatory Affairs for the UK & Ireland. The role is fully remote within the UK, leading the UK RA team, shaping MAA strategies, and ensuring UK and Ireland regulatory compliance throughout development and lifecycle management.

The candidate will have extensive MHRA experience, a track record in oncology MAAs, and at least 8 years in regulatory roles within the biopharmaceutical sector. Advanced degree is preferred.

Qualifications

• Minimum of 8 years’ experience in the biotechnical or pharmaceutical industry, and a minimum of 8 years’ experience in a Regulatory capacity.
• Experience working with MHRA regulatory procedures is mandatory for this role.
• Strong understanding of UK regulatory requirements and policy trends.
• Experience with oncology products and MAAs is preferred.

Responsibilities

• Lead the UK RA team to manage regulatory aspects of designated compounds through development, registration, post-approval, and lifecycle.
• Define UK MAA strategy aligned with product development objectives.
• Prepare UK MAA dossiers and ensure compliance with UK and Ireland requirements.
• Serve as the UK regulatory liaison within senior leadership and coordinate with EU RA for clinical matters.
• Represent regulatory affairs at meetings and industry associations, and mentor junior staff.

Skills

Regulatory strategy

MHRA experience

Leadership

Cross-functional collaboration

Education

Bachelor’s degree

Advanced degree preferred

Tools

Microsoft Office

Veeva regulatory publishing

PowerPoint

Job description

## Associate Director, Regulatory Affairs - UK & IrelandApply: United Kingdom Remote: Full time: Posted Today: R35200BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.**General Description:**The Associate Director of Regulatory Affairs will be responsible for developing and implementing UK regulatory strategies for development programs to secure and maintain the marketing authorization for product(s) in line with business objectives, and in coordination with key internal stakeholders. This will also include oversight and management of commercial products for both UK and Ireland.**Essential Functions of the job:**This individual will lead the UK RA team to manage regulatory aspects of designated compounds (NME/New indications) through all phases of development, registration, post-approval, and lifecycle of the product as detailed below:* Collaborate with key internal stakeholders to define UK MAA strategy and ensure the regulatory strategy is incorporated and implemented in line with product development objectives* Manage the content of and prepare regulatory (UK MAA) dossiers. Have knowledge of the content of the EU MAA dossiers to support labeling updates and management in Ireland ensuring compliance with UK and Ireland regulatory requirements. Oversee and be accountable for regulatory agency communications, submissions, and approvals, with a quality focus to secure first-cycle/attempt approvals* Review and provide input into promotional materials for both UK and Ireland* Act as the RA liaison within the UK Leadership team, attend regular meetings and provide input into UK business strategy* Prepare team for HA interactions, and moderate and lead discussions, be the main MHRA contact for strategic, non-study specific topics and provide support to the EU RA team for clinical matters related to Health Authority topics.* Proactively anticipate and mitigate regulatory risks while maintaining current knowledge of regulatory intelligence, procedures, changes, and trends.* Provide submission gap analyses, identify potential risks and propose potential solutions/mitigation plans to ensure successful acceptance of submissions.* Ensure compliance with EU/UK global regulatory requirements.* To lead and mentor junior team members.* Represent BeOne at UK industrial association meetings and congresses**Supervisory Responsibilities:*** Junior Regulatory Affairs professionals**Computer Skills:** Extensive experience with Microsoft Office suite, Veeva regulatory publishing and expertise with PowerPoint presentation authoring and presentation.**Education Required:**Bachelor’s degree required; advanced degree preferred.**Other Qualifications:*** Minimum of 8 years’ experience in the biotechnical or pharmaceutical industry, and a minimum of 8 years’ experience in a Regulatory capacity with a broad background.* Experience working with MHRA regulatory procedures is mandatory for this role.* Sound understanding of the drug development process, the pharmaceutical industry and healthcare environment including UK regulatory requirements and policy trends* Recent experience with oncology products and MAAs, ODD, PIP is preferred* Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism**Location:** UK, fully remote**Travel:** Travel to internal meetings in UK monthly or bimonthly. Additional travel to EU locations occasionallySalary Range UK: 80,700.00 GBP - 100,900.00 GBP