RIM Analyst: Global Pharma Data & Submissions (Remote)

SRG; Maidenhead; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading global pharmaceutical company is seeking a Regulatory Information Management (RIM) Analyst for a hybrid position in Maidenhead. This role involves managing data remediation and improving processes in regulatory information management. Ideal candidates should have 1-2 years of experience in regulatory systems, hands-on knowledge of xEVMPD/IDMP, and good communication skills. This is a temporary role for an initial 12-month contract with a pay rate of circa £23 per hour. Apply now to join this dynamic team.

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 for COSMOS data management.
• Lead small-scale system/process improvement projects.
• Support xEVMPD/IDMP data submissions.

Skills

Hands-on experience with RIM or regulatory systems

Knowledge of regulatory business processes

Strong organizational skills

Communication skills

Interpersonal skills

Ability to manage competing deadlines

Education

Graduate in a Life Sciences or IT discipline

Job description

A leading global pharmaceutical company is seeking a Regulatory Information Management (RIM) Analyst for a hybrid position in Maidenhead. This role involves managing data remediation and improving processes in regulatory information management. Ideal candidates should have 1-2 years of experience in regulatory systems, hands-on knowledge of xEVMPD/IDMP, and good communication skills. This is a temporary role for an initial 12-month contract with a pay rate of circa £23 per hour. Apply now to join this dynamic team.