Senior Manager, Regulatory Information Management (Remote)

Jazz Pharmaceuticals; Oxford; Remote; GBP 95,000 - 143,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Senior Manager for Regulatory Information Management to oversee RIM system training and documentation. The role requires at least 5 years of experience in Pharmaceutical Affairs and a Bachelor's Degree in a relevant field. The ideal candidate will possess strong project management skills and knowledge of regulatory requirements. This position offers a competitive compensation package and remote work flexibility.

Benefits

Competitive base pay

Potential bonuses

Equity grants

Qualifications

• Minimum of 5 years of experience in Pharmaceutical/Regulatory Affairs.
• Ability to manage timely project deliveries.

Responsibilities

• Manage training, documentation, and maintenance of the RIM system.
• Configure RIM environments and gather user requirements.
• Develop and implement data and document migration strategies.

Skills

Pharmaceutical/Regulatory Affairs experience

Project management skills

Exceptional written and verbal communication skills

Understanding of US/EU/International Regulatory Requirements

Education

Bachelor's Degree in Business or Life Sciences

Tools

Veeva

Job description

Job Title: Senior Manager, Regulatory Information Management (Remote), Oxford

Client:

Jazz Pharmaceuticals

Location:

Oxford, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

0edf41a6dc17

Job Views:

11

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

Required Knowledge, Skills, and Abilities:

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

Required/Preferred Education and Licenses:

• Bachelor's Degree in Business or Life Sciences.

Jazz Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, disability, veteran status, or any characteristic protected by law.

Compensation and Benefits (US-based candidates):

The base pay range is $128,000-$192,000, depending on qualifications and experience. Additional benefits include potential bonuses, incentives, and equity grants. Benefits offerings vary and are detailed in the full benefits package.