At a Glance
- Tasks: Lead regulatory strategies and ensure compliance for clinical development programmes.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, professional growth, and a values-driven work culture.
- Other info: Opportunity to mentor a team and collaborate with cross-functional experts.
- Why this job: Make a real impact on patient care by driving regulatory affairs performance.
- Qualifications: Significant regulatory affairs experience and strong leadership skills required.
The predicted salary is between 63000 - 77000 £ per year.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Director, Regulatory Affairs at ICON, you will develop and execute regulatory strategies, ensuring compliance with global regulations, and facilitate the successful submission and approval of clinical development programs.
What You Will Do
- Drive regulatory affairs performance, ensuring quality, and building capability across your area.
- Lead and oversee the regulatory affairs strategy for ICON's therapeutic area teams.
- Collaborate with cross-functional teams to develop comprehensive regulatory plans and submissions.
- Provide expert guidance on regulatory requirements and ensure adherence to global regulations.
- Represent ICON in interactions with regulatory authorities, presenting data and addressing inquiries.
- Mentor and develop a team of regulatory affairs professionals, fostering their growth and expertise.
Your Profile
- Significant regulatory affairs experience, with a track record of building high-performing teams and delivering results.
- Bachelor's degree in a relevant scientific discipline or healthcare-related field; advanced degree preferred.
- Extensive experience in regulatory affairs, with a proven track record in leading global submissions.
- In-depth knowledge of regulatory guidelines, ICH/GCP, and industry best practices.
- Strong analytical and problem-solving skills, with the ability to navigate complex regulatory landscapes.
- Excellent communication and negotiation abilities, with the capacity to convey regulatory strategies effectively.
- Willingness to travel as required (approximately 25%).
Senior Director, Regulatory Affairs employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
