General Description:

The Director, Regulatory Affairs, Dx/CDx and Medical Devices will be responsible for leading a small team for developing and implementing regulatory diagnostic and medical device strategies as applicable, for the designated program to support clinical trials where necessary, and facilitate marketing authorization in line with business objectives, and in coordination with key internal and external stakeholders.

Essential Functions of the job:

Develop European and/or UK regulatory strategy for the designated program, and contribute to the clinical development plans to align diagnostic testing and drive integration to therapeutic development plans.

Act as the representative of European regulatory team at the global regulatory team (GRT) for the designated projects needing diagnostics, and may also be required to represent diagnostic strategies to global cross-functional teams for specific topics

Drive the strategy, providing direction and oversight for Dx/CDx and Device related content of regulatory documents, such as, CPS, CPSR, IBs, and briefing documents for interactions with European regulatory authorities or RFIs, as applicable.

Provide submission gap analyses, identify potential risks and propose potential solutions/mitigation plans to ensure successful acceptance of diagnostic submissions

Oversee and be accountable for Dx/CDx and Device related regulatory agency communications, submissions, and approvals, with a quality focus to minimize cyclical review

Lead and mentor team members

Maintain up-to-date working knowledge of laws, regulations, and guidelines across the European regulatory authorities and the UK.

Represent the BeOne European regulatory function at industry consortium (may be required).

Qualifications:

Minimum of 10+ years’ experience in the biotechnical or pharmaceutical industry with a bachelor's degree, and a minimum of 10 years’ experience in a Regulatory capacity with increasing responsibility.

Seasoned negotiator, both internally and externally with a solid background in medical devices/diagnostic development regulations and associated regulatory deliverables.

Experience working with Notified Bodies and various Member State HAs to support diagnostic testing.

Sound understanding of the drug and diagnostic development process, the pharmaceutical industry and healthcare environment including Global and EU/UK regulatory requirements and policy trends

Recent experience with diagnostic testing to support clinical trials in all phases of study, is mandatory for this role.

Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism

English native speaker is preferred and remote working possible

Location: Remote

Reports To: Executive Director, Global Regulatory Strategy, Dx/CDx and Medical Devices.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.