Cambridge Hybrid: Regulatory Data & Systems Lead (RIM/Veeva)

Mundipharma International; Cambridge; Hybrid; GBP 125,000 - GBP 150,000; Full time

Job summary

A global healthcare company is seeking a Regulatory Affairs Systems and Data Manager based in Cambridge (Hybrid/Flexible). You will manage regulatory information systems, drive compliance with Veeva Vault RIM, and oversee training and SOP development. The ideal candidate will have proven experience in regulatory operations within the pharmaceutical industry and excellent communication skills. This position offers a collaborative work environment and flexible benefits.

Benefits

Flexible benefits package

Opportunities for learning & development

Collaborative, inclusive work environment

Qualifications

• Proven experience in a regulatory operations function within the pharmaceutical industry.
• Understanding of global regulatory requirements and compliance standards.
• Able to work in a dynamic and fast-paced environment.

Responsibilities

• Accountable for strategy and management of regulatory information management systems.
• Develop reporting mechanisms for compliance oversight.
• Set up and update regulatory affairs SOPs.
• Oversee submission management activities.

Skills

Experience in pharmaceutical regulatory operations

Proficiency in Veeva Vault RIM

Excellent communication skills

Ability to solve problems proactively

Tools

Veeva Vault RIM

Data analytics and reporting tools

Job description

A global healthcare company is seeking a Regulatory Affairs Systems and Data Manager based in Cambridge (Hybrid/Flexible). You will manage regulatory information systems, drive compliance with Veeva Vault RIM, and oversee training and SOP development. The ideal candidate will have proven experience in regulatory operations within the pharmaceutical industry and excellent communication skills. This position offers a collaborative work environment and flexible benefits.