Analyst, Regulatory Information Management

SRG; Thatcham; Hybrid; GBP 60,000 - 80,000; Part time

Job summary

A leading global pharmaceutical company is looking for a Regulatory Information Management (RIM) Analyst to support global systems and processes. The role is a temporary position for an initial 12 months and includes managing data remediation and driving process improvements. The ideal candidate should have a background in Life Sciences or IT, with 1-2 years of experience in regulatory systems. Strong communication and organizational skills are essential. The job is hybrid, located in Maidenhead.

Qualifications

• 1-2 years of hands‑on experience with RIM or regulatory systems.
• Experience as a super user or trainer on major systems or structured data topics (xEVMPD/IDMP).

Responsibilities

• Maintain compliance with SOPs and work instructions for COSMOS data management.
• Lead small-scale system/process improvement projects.
• Support xEVMPD/IDMP data submissions to meet regulatory requirements.
• Collaborate with global regulatory teams.

Skills

Hands-on experience with RIM

Knowledge of regulatory business processes

Strong organizational skills

Communication skills

Interpersonal skills

Education

Graduate in Life Sciences or IT

Job description

Analyst, Regulatory Information Management

Department: Regulatory Affairs

Location: Maidenhead/Remote (hybrid)

Employment Type: Temporary - 12 month initial

Rate: circa £23 per hour (PAYE)

Role Summary

We are seeking a Regulatory Information Management (RIM) Analyst to support global RIM systems and processes for a leading global pharmaceutical company. This role is an initial 12 month contract and will involve managing data remediation, structured data submissions (xEVMPD, IDMP), and driving process improvements. You will collaborate with global regulatory teams, lead small-scale initiatives, and mentor junior colleagues to ensure compliance and efficiency in regulatory information management.

Key Responsibilities

• Maintain compliance with SOPs and work instructions for COSMOS data management and submissions.
• Lead small-scale system/process improvement projects and act as a point of contact for technical queries.
• Support xEVMPD/IDMP data submissions and SPOR maintenance to meet regulatory requirements.
• Resolve moderate data or archiving issues independently and recommend solutions.
• Collaborate with global regulatory teams to ensure effective communication and implementation of RIM processes.
• Participate in projects for data submission standards (e.g., IDMP, PQ CMC, SPQS).

Experience & Skills Required

• Graduate in a Life Sciences or IT discipline (and/or equivalent experience).
• 1-2 years of hands‑on experience with RIM or regulatory systems.
• Knowledge of regulatory business processes and European regulatory procedures.
• Experience as a super user or trainer on major systems or structured data topics (xEVMPD/IDMP).
• Strong organizational, communication, and interpersonal skills.
• Ability to lead small team discussions and manage competing deadlines effectively.

To Apply

If you are interested and want