Student Placement Associate Specialist, Regional Regulatory Operations, EU + EEMEA

Job Description

This role will be based in our modern state‑of‑the‑art co‑working facilities in Moorgate, London. The site, at the heart of London, provides fantastic amenities, support services and collaborative workspaces with convenient transport links.

Brief Description of Position

You will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organisation in the Regulatory Affairs Operations International team, which is based in Europe.

You will support the regulatory submission creation and the registration tracking of the company regulatory submission targets from a regulatory operational perspective across the Europe, Middle East and Africa regions (EU & EEMEA).

As a member of a cross‑functional team for the assigned products you will support the team to manage all operational aspects for submission planning and execution of Original Marketing Application (OMA) and post‑approval regulatory changes.

This position requires a keen interest in the regulatory landscape, its registration procedures and a willingness to understand the technical requirements for dossiers.

Primary Activities

• Support the planning and management of regulatory operation projects from authorisation through delivery to country regulatory affairs teams and/or Health Authorities.
• Support the regulatory submission plan for the assigned projects/products and maintain the related project milestones.
• Participate in cross‑functional forums and meetings.
• With manager support drive the submission assembly and delivery process with the Global and/or Regional Submission Publishing team to ensure timely assembly, publishing and archival of assigned products/submissions as per the agreed timelines.
• Access and maintain the regulatory systems and databases to fulfil daily functions.
• Identify opportunities to continually improve the efficiency of the submission processes and systems and participate in small‑scale process improvement projects.
• Learn knowledge of the regional regulatory procedures on internal and external guidelines and standards.

Qualifications

You must be currently studying at a UK university and will be looking to complete a 12‑month student internship as part of your undergraduate degree.

Technical requirements are flexible but an affinity for and capability to learn Regulatory Information Management systems to execute operational tasks will be a significant asset.

How to Apply

Please complete the online application form by answering the questions within the application and upload your CV and Cover Letter in a combined document in the resume/CV section.

The standard Future Talent recruitment process is: an online application, a virtual conversation and then a final assessment.

Next Steps

In the event of your successful progression to the next stage, one of our future talent team members will contact you within two–three weeks of the application closing date.

Start Date: June 2026

Equal Opportunity Employer

We are proud to be a company that embraces the value of bringing diverse, talented and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer committed to fostering an inclusive and diverse workplace.

Job Posting End Date: 10/07/2025

Employment Type: Full‑Time

Employee Status: Intern / Co‑op (Fixed Term)

Relocation: VISA Sponsorship

Contact: future talent page reference omitted for compliance