Senior Global Regulatory Affairs Specialist

This is a fully remote position, open to applicants in United Kingdom, +4 more countries.

📋 Description

• Formulate global regulatory strategies to ensure the successful submission and approval of clinical trial applications and marketing authorizations.

• Offer regulatory guidance and support to cross-functional teams throughout the drug development lifecycle.

• Guarantee compliance with international regulatory requirements and standards.

• Oversee regulatory submissions and liaise with health authorities.

• Engage in regulatory intelligence activities to remain informed about changes in regulations and guidelines.

• Assume responsibility for regulatory affairs deliverables and leverage expertise to tackle complex challenges.

⛳️ Requirements

• Bachelor’s degree in a scientific discipline or a related field.

• At least 5 years of experience in regulatory affairs within the pharmaceutical or biotechnology sectors.

• Profound understanding of global regulatory requirements and guidelines.

• Exceptional communication and interpersonal skills.

• Capability to work both independently and collaboratively in a dynamic environment.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career progression pathways.