(Senior) Regulatory Manager at Precision for Medicine

Precision for Medicine is seeking a Regulatory Manager to contribute to their team. This role is available for candidates based in the UK, Spain, Hungary, Slovakia, Serbia, Romania, or Poland. The Regulatory Manager will be responsible for providing regulatory strategy and development guidance for clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures. They will ensure the timely preparation of high-quality regulatory submissions in compliance with regulations.

The Regulatory Manager will coordinate and prepare regulatory documents for submission to Regulatory Authorities and/or Ethics Committees.

Role Involves:

• Providing regulatory guidance throughout the clinical development life cycle
• Compiling, coordinating, and reviewing applications to Regulatory Authorities
• Developing and reviewing documents for submission to Regulatory Authorities and/or Ethics Committees
• Serving as a representative of Global Regulatory Affairs at project team meetings
• Overseeing and coordinating Regulatory Affairs Specialists
• Maintaining project plans, project trackers, and regulatory intelligence tools
• Assisting in the development of Regulatory Affairs Specialists
• Providing input into regulatory strategy and timeline development
• Participating in corporate quality initiatives
• Staying updated on laws, regulations, and guidelines governing drug development and approval
• Providing ICH GCP guidance, advice, and training
• Serving as a representative of Global Regulatory Affairs at business development meetings

Requirements:

• Bachelor's degree in a scientific or healthcare discipline
• 5 years (Manager) or 7 years (Senior Manager) of regulatory experience
• Computer literacy (MS Office/ Office 365)
• Fluency in English
• Regulatory affairs experience working for a Clinical Research Organisation
• Experience leading Clinical Submissions
• Knowledge of drug development process and regulatory activities for at least one major region (EU, US)
• Ability to understand clinical and pre-clinical study results
• Knowledge of clinical trials methodology
• Knowledge and expertise with relevant regulations and guidance
• Availability for domestic and international travel

Role Offers:

• Opportunity to work remotely
• Chance to contribute to groundbreaking cancer therapies
• Valued input and ideas impacting positive change for the company