Manager - Regulatory Affairs Submission Management

Contract: Temporary - 12 months (extension possible)
Location: Maidenhead - hybrid working (or remote if needed)
Rate: (INSIDE IR35)
- circa. £22-25 per hour (PAYE)*

SRG are seeking a Regulatory Affairs professional with Submission Management skills & experience to assist a leading pharmaceutical company on a temporary basis. Join a dynamic regulatory affairs team and play a pivotal role in delivering complex regulatory submissions that support the development, approval, and life-cycle management of innovative healthcare products.

Key Responsibilities

• Lead and manage complex regulatory submission projects, ensuring high-quality dossiers are delivered on time and in line with regulatory requirements.
• Act as the primary regulatory submission management contact for cross-functional project teams, providing guidance on processes, timelines, and deliverables.
• Coordinate and facilitate submission planning meetings, driving progress across multiple concurrent projects and stakeholders.
• Oversee publishing activities and collaborate with external publishing partners to ensure successful submission delivery.
• Perform quality reviews of published submissions, ensuring compliance with technical standards and regulatory authority requirements.
• Contribute to continuous improvement initiatives, enhancing regulatory processes, standards, and systems.

Skills & Experience Required

• Bachelor's degree or equivalent combination of education and relevant industry experience.
• Experience within the pharmaceutical, biotechnology, healthcare, or related regulated industry.
• Strong project management skills, with experience managing complex, cross-functional activities and competing priorities.
• Knowledge of regulatory operations, submission management, and/or submission publishing processes.
• Excellent written and verbal communication skills, with the ability to influence stakeholders in a matrix environment.
• Demonstrated leadership capability, including mentoring colleagues and driving process improvements. PMP and/or RAC certification is advantageous.

To Apply

Please click and submit your profile and/or to discuss further, contact Theo Charles on 07836 251472

*Umbrella also possible - please enquire for more information

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.