Senior Manager, Regulatory Information Management (Remote)

Jazz Pharmaceuticals; London; Remote; GBP 70,000 - 100,000; Full time

Job summary

A leading pharmaceutical company is looking for a Senior Manager in Regulatory Information Management based in London. This remote role involves collaborating with R&D and Manufacturing teams to enhance the RIM system. Responsibilities include configuration management, user support, and training development, aimed at ensuring compliance with regulatory standards.

Qualifications

• Minimum 5 years in pharmaceutical or Regulatory Affairs.
• Knowledge of US, EU, and international regulatory requirements.

Responsibilities

• Configure RIM environments based on approved proposals.
• Manage user accounts and permissions associated with RIM.
• Create and deliver tailored RIM training materials.

Skills

Regulatory Affairs Experience

Communication Skills

Project Management

Education

Bachelor's Degree in Business or Life Sciences

Job description

Social network you want to login/join with:

Senior Manager, Regulatory Information Management (Remote), London

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 5fbb67a82195

Job Views: 9

Posted: 22.06.2025

Expiry Date: 06.08.2025

Job Description:

Brief Description:

The Senior Manager, Regulatory Information Management (RIM), will work closely with R&D and Manufacturing, as well as other functions within Jazz, to manage training, documentation, user experience, and maintenance of the RIM system and its integration with other systems at Jazz.

Essential Functions:

• Understand business processes across R&D and Manufacturing, regulatory, and reporting requirements, and translate these into RIM configuration ideas and proposals.
• Configure RIM environments (Sandbox, Validation, and Production) according to approved proposals.
• Collaborate with other Business and System Leads at Jazz to ensure data alignment, system configuration consistency, and optimal user experience.
• Gather user requirements and create end-user reports.
• Support triage requests from users across GRA and Manufacturing.
• Develop and implement data and document migration strategies.
• Manage RIM user accounts in conjunction with IT, including permissions and security profiles.
• Create and deliver RIM training materials tailored to different knowledge levels within R&D and Manufacturing.
• Maintain knowledge of systems outside of RIM, such as Publishing.

Required Knowledge, Skills, and Abilities:

• Minimum of 5 years’ experience in pharmaceutical or Regulatory Affairs, with relevant education.
• Knowledge of US, EU, and international regulatory requirements.
• Ability to manage timely project and program delivery.
• Exceptional written and verbal communication skills.

Required/Preferred Education and Licenses:

• Bachelor's Degree in Business or Life Sciences is required.