Senior Manager, Regulatory Information Management (Remote)

Jazz Pharmaceuticals; London; Remote; GBP 70,000 - 90,000; Full time

Job summary

A global pharmaceutical company in London is seeking a Senior Manager for Regulatory Information Management to oversee training, documentation, and system integration. The ideal candidate has over 5 years of experience in pharmaceutical regulatory affairs and excels in project management and communication. The position is remote with competitive benefits.

Qualifications

• Minimum 5 years of pharmaceutical/Regulatory Affairs experience with relevant education.
• Knowledge of US/EU/International Regulatory Requirements.
• Ability to manage timely delivery of projects and programs.
• Exceptional written and verbal communication skills.

Responsibilities

• Understand the business processes across R&D and Manufacturing.
• Configure RIM as per agreed proposals.
• Collaborate with Business and System Leads across Jazz.
• Gather user requirements and create end-user reports.
• Support triage requests from users.
• Develop and deliver data and document migration strategies.
• Manage RIM user accounts and permissions.
• Create and deliver RIM training materials.
• Maintain knowledge of systems outside of RIM.

Skills

Pharmaceutical/Regulatory Affairs experience

Knowledge of US/EU/International Regulatory Requirements

Project management

Written and verbal communication skills

Education

Bachelor's Degree in Business or Life Sciences

Job description

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Senior Manager, Regulatory Information Management (Remote), London

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 5fbb67a82195

Job Views: 16

Posted: 12.08.2025

Expiry Date: 26.09.2025

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

1. Understand the business processes (across R&D and Manufacturing), regulatory and reporting requirements, and convert these into RIM configuration ideas/proposals.
2. Configure RIM (Sandbox, Validation, and Production environments) as per the agreed proposals.
3. Collaborate with other Business and System Leads across Jazz to ensure alignment of data, system configurations, and user experience.
4. Gather user requirements and create end-user reports.
5. Support triage requests from users across GRA and Manufacturing.
6. Develop and deliver data and document migration strategies.
7. Manage RIM user accounts (in conjunction with IT), including permissions and security profiles.
8. Create and deliver RIM training materials tailored to different knowledge and experience levels across R&D and Manufacturing.
9. Maintain knowledge of systems outside of RIM, including Publishing.

Required Knowledge, Skills, and Abilities

1. Minimum 5 years of pharmaceutical/Regulatory Affairs experience with relevant education.
2. Knowledge of US/EU/International Regulatory Requirements.
3. Ability to manage timely delivery of projects and programs.
4. Exceptional written and verbal communication skills.

Required/Preferred Education and Licenses

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