Global Regulatory Submissions Lead — Pharma

SRG; Stone Cross; On-site; GBP 60,000 - 85,000; Full time

Job summary

SRG is seeking an experienced Hub Submission Manager to join a global regulatory operations team within a highly regulated pharmaceutical environment. The role focuses on managing regional and national submissions from planning to archival to ensure compliant, timely delivery.

You will coordinate activities across markets, drive improvements in submission processes, and provide expertise to colleagues and project teams in a fast-paced setting.

Qualifications

• Experience coordinating regulatory submissions in pharma, biotech, or life sciences.
• Strong project management and organisational skills across multiple priorities.
• Knowledge of regional and national filing guidelines and dossier structures.
• Experience with electronic submission systems and regulatory technologies.
• Bachelor's degree in Pharmacy or Life Sciences, or equivalent experience.
• Excellent communication and stakeholder management across global teams.

Responsibilities

• Lead and coordinate regulatory submission activities for products and markets.
• Plan, compile, build, and deliver electronic and paper dossiers to authorities.
• Collaborate with regulatory teams, country reps and external stakeholders on requirements and timelines.
• Monitor milestones and resolve issues impacting delivery schedules.
• Drive process improvement and regulatory technology advancements.
• Act as subject matter expert, providing guidance and training.

Skills

Regulatory submissions

Project management

Stakeholder management

Electronic submission systems

Regulatory technologies

Education

Bachelor's degree in Pharmacy

Life Sciences or related discipline

Tools

Electronic submission systems

Document management platforms

Job description

SRG is seeking an experienced Hub Submission Manager to join a global regulatory operations team within a highly regulated pharmaceutical environment. The role focuses on managing regional and national submissions from planning to archival to ensure compliant, timely delivery.

You will coordinate activities across markets, drive improvements in submission processes, and provide expertise to colleagues and project teams in a fast-paced setting.