Senior Director Regulatory Affairs

CompanyClinigen

LocationWeybridge, England, United Kingdom

Posted At1/15/2026

UK Visa Sponsorship Analytics

Occupation Type

Quality assurance and regulatory professionals

Occupation Code Skill LevelHigher Skilled

Sponsorship Salary Threshold

£48,200 (£24.72 per hour)

Occupation rate applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with Clinigen. For the most up-to-date job details, please visit the official website by clicking "Apply Now."

Description

Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned well for an exciting future of continued expansion.

We have a newly created a high-impact leadership role for a senior Regulatory Affairs professional who wants to shape strategy, influence clients and drive business growth. Acting as Deputy to the Regulatory Affairs function, you will be a trusted regulatory partner to both internal stakeholders and global clients, leading the delivery of complex regulatory projects from strategy through to execution.

You will play a pivotal role in guiding regulatory pathways for marketing authorisations and managed access programs, while also supporting business development by helping win and grow client relationships. Combining deep regulatory expertise with commercial awareness, you will translate regulatory intelligence into clear, actionable advice that enables compliant, timely access to medicines and supports Clinigen’s continued growth.

Operational

Act as the deputy for Regulatory Affairs function.
Assist in managing the workload and resource levels needed to support the business division.
Represent Clinigen professionally in external meetings in a variety of contexts (regulatory authorities, conferences, business meetings).
Delivery of department-relevant projects to meet business needs.
Responsible for allocated products including applications for marketing authorizations in new territories and maintenance of existing licences.
Responsible for the provision of regulatory affairs support for allocated projects such as Managed Access programs, commercial partnerships, standalone projects.
Responsible for supporting regulatory Due Diligence of potential acquisitions/partnered product opportunities etc.
Responsible for supporting the development of regulatory strategies and provision of regulatory advice internally and externally.

Leadership

Support the operational growth and expansion of the PV/MI/RA division in line with the company’s strategy.
Develop and nurture the Regulatory Affairs team to consistently provide high standard regulatory support across all business divisions.

Be a key client contact to represent Clinigen externally and deliver client projects.

Promote and act to protect patient and public health and regulatory compliance.

Regulatory Intelligence and Compliance

Ensure that all regulatory activities comply with current Regulatory Agencies’ requirements and guidelines.
Support the maintenance the Regulatory Intelligence repository for the supply of unlicensed medicines.
Ensure Regulatory Intelligence updates are effectively communicated within the company highlighting business impact to help ensure regulatory compliance and proper planning.
Proactively builds/strengthens contact with external stakeholder (Regulatory Agency, external experts, commercial partners etc.) to help achieve strategic goals and objectives.
Contribute to company SOPs for PV/MI/RA.

Key Requirements:

Bachelor's Degree in Life Sciences or scientific discipline
Significant experience gained working in Regulatory Affairs within pharmaceutical industry/CRO
Relevant experience in a client facing role
Wide experience and knowledge of Regulatory Affairs with an excellent grounding in European procedures and ideally exposure to medicines access i.e. expanded access/compassionate use/ drug development or RoW experience

Understanding of clinical research and clinical trials

Demonstrate ability to deliver results to the appropriate quality, budget and timeline metrics

Proven ability to successfully manage global regulatory projects

Proven ability to provide coaching, advice and mentoring in areas of Regulatory Affairs

Excellent organisational and project management skills

Confident dealing with managers and employees at all levels

Outstanding written, verbal and interpersonal communications skills

Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment

Ability to be effective in the business development setting, with strong presentation skills

Effective communicator and influencer across all mediums

Benefits:

27 days holiday, plus bank holidays
Discretionary Bonus
Private Health
Pension contributions & Life Assurance scheme
Flexible Benefits Platform
Annual salary review
Independent financial advice service
Enhanced Employee Assistance Programme
Shopping discounts with retailers
Long service awards
Recognition scheme & employee of the year awards

Interested? We would love to hear from you, please apply today for consideration.