At a Glance
- Tasks: Lead global regulatory strategy for innovative clinical-stage programmes in Oncology.
- Company: Dynamic biotechnology company focused on cutting-edge therapies.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Join a collaborative team dedicated to advancing innovative therapies in oncology.
- Why this job: Make a significant impact in global health by shaping regulatory pathways for breakthrough treatments.
- Qualifications: Extensive experience in Regulatory Affairs with a focus on FDA and EMA interactions.
The predicted salary is between 51750 - 63250 £ per year.
About the Role
An innovative biotechnology company is seeking an experienced regulatory professional to lead global regulatory strategy across a portfolio of clinical-stage programmes.
This is a highly strategic role, providing regulatory leadership across development activities and acting as the key regulatory partner to cross-functional teams.
The successful candidate will be responsible for driving regulatory strategy across the US, Europe and international markets whilst supporting development programmes from early clinical development through to registration.
Key Responsibilities
- Lead and execute global regulatory strategies for assigned development programmes in Oncology.
- Provide regulatory leadership across FDA, EMA and international markets.
- Act as the regulatory representative on cross-functional project teams.
- Lead interactions with Health Authorities, including FDA and EMA.
- Provide strategic input into clinical development plans and regulatory pathways.
- Support preparation and review of key regulatory submissions.
- Assess regulatory risks and develop mitigation strategies.
- Ensure regulatory activities are aligned with programme objectives and timelines.
Experience Required
- Significant Regulatory Affairs experience within biotechnology or pharmaceutical development.
- Proven experience leading global regulatory strategy for innovative products.
- Strong experience supporting clinical development programmes from Phase I through Phase III.
- Hands-on strategic experience with IND, CTAs and BLA submissions is essential.
- Strong knowledge of FDA and EMA regulatory requirements.
- Experience leading Health Authority meetings and regulatory interactions.
- Excellent stakeholder management and communication skills.
- Ability to influence programme strategy within a cross-functional environment.
- Ideal Background
Suitable for an experienced regulatory leader with a strong track record in global clinical development, regulatory strategy, FDA and EMA interactions, and major regulatory submissions.
Experience in oncology, biologics, immunology or other innovative therapeutic areas would be highly advantageous.
Regulatory Director Contract - Global Lead - US EU in London employer: Hays Specialist Recruitment Limited Careers
Hays Education is an exceptional employer, offering a supportive and collaborative work environment for SEN SLD/PMLD teachers in the Hounslow/Hillingdon area. With access to exclusive vacancies, ongoing professional development, and a dedicated consultant to guide your career, you will find ample opportunities for growth while making a meaningful impact on the lives of pupils with special educational needs. Join us to be part of a community that values inclusivity and fosters both personal and professional development.
Contact Details:
Hays Specialist Recruitment Limited Careers Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Director Contract - Global Lead - US EU in London
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We think you need these skills to ace Regulatory Director Contract - Global Lead - US EU in London
Some tips for your application 🫡
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