Senior Regulatory Project Manager

Responsibilities

• Develop and implement regulatory strategies for global clinical trials
• Provide expertise and guidance on regulatory requirements and compliance issues
• Collaborate cross-functionally with teams to ensure regulatory objectives are met
• Lead interactions with regulatory agencies and prepare submissions
• Keep abreast of regulatory updates and industry trends to inform strategy

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Minimum of 5 years of experience in regulatory affairs within the pharmaceutical or biotech industry
• Strong knowledge of global regulatory requirements and guidelines
• Prominent track record of successful regulatory submissions and interactions
• Excellent communication, leadership, and problem-solving skills

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways