Senior Manager, Regulatory Information Management (Remote)

Jazz Pharmaceuticals; Oxford; Remote; USD 128,000 - 192,000; Full time

Job summary

A leading company in pharmaceuticals is seeking a Senior Manager in Regulatory Information Management to enhance user experiences, manage regulatory documentation, and implement training programs. The ideal candidate will possess a strong project management background, deep knowledge of regulatory requirements, and comprehensive experience in the pharmaceutical industry.

Benefits

Potential bonuses

Incentives and other offerings

Qualifications

• Minimum 5 years of pharmaceutical/Regulatory Affairs experience.
• Veeva White Belt certification required.
• Knowledge of US/EU/International Regulatory Requirements is necessary.

Responsibilities

• Manage training, documentation, and maintenance of the RIM system.
• Gather user requirements and create end-user reports.
• Develop data and document migration strategies.

Skills

Project Management

Communication

Education

Bachelor's Degree in Business or Life Sciences

Tools

Veeva

Job description

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

Company:

Jazz Pharmaceuticals

Location:

Oxford, United Kingdom

Job Category:

Other

Job Reference:

0edf41a6dc17

Job Views:

47

Posted Date:

24.06.2025

Expiry Date:

08.08.2025

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 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/proposals.
• Configure RIM (Sandbox, Validation, and Production environments) according to approved proposals.
• Collaborate with Business and System Leads to ensure data alignment, system configuration consistency, and optimal user experience.
• Gather user requirements and create end-user reports.
• Support user requests across GRA and Manufacturing.
• Develop and implement data and document migration strategies.
• Manage RIM user accounts, permissions, and security profiles in conjunction with IT.
• Create and deliver RIM training materials tailored to various knowledge levels.
• Maintain knowledge of other relevant systems outside of RIM.

Required Knowledge, Skills, and Abilities:

• Minimum 5 years of pharmaceutical/Regulatory Affairs experience with a Bachelor's Degree in Business or Life Sciences.
• Veeva White Belt certification.
• Knowledge of US/EU/International Regulatory Requirements.
• Strong project management skills and excellent communication skills.

Additional Information:

Jazz Pharmaceuticals is an equal opportunity employer. Compensation ranges from $128,000 to $192,000, depending on qualifications and experience. Benefits include potential bonuses, incentives, and other offerings.