Regulatory Affairs Systems and Data Manager

Mundipharma Research Limited; Cambridge; Hybrid; GBP 90,000 - 130,000; Full time

Benefits offered by this job

Flexible benefits package

Learning & development opportunities

Collaborative, inclusive work culture

Job summary

Mundipharma Research Limited in Cambridge is seeking a Regulatory Affairs & Systems Data Manager to lead strategy and governance of the regulatory information management system and data across the regulatory function.

You will oversee Veeva Vault RIM implementation, drive compliance improvements, and collaborate with IT and business partners to integrate RIM across the organization, while developing training and SOPs.

Qualifications

• Experience in regulatory operations within the pharmaceutical industry.
• Proficiency with Veeva Vault RIM and implementing its enhancements.
• Understanding global regulatory requirements and compliance standards.
• Ability to work independently and solve problems proactively.
• Strong written and verbal communication skills.

Responsibilities

• Strategic oversight of the regulatory information management system.
• Oversee implementation and optimization of Veeva RIM.
• Develop regulatory data management to ensure compliance.
• Collaborate with stakeholders to integrate RIM across the business.
• Budget assessment for regulatory data management.
• Train users and develop SOPs for Veeva and RIM activities.
• Lead submission management and publishing teams.

Skills

Regulatory strategy

Data analytics

Communication

Independent work

Tools

Veeva Vault RIM

Job description

Regulatory Affairs & Systems Data Manager

Location: Cambridge (Hybrid/Flexible) Job type: Permanent

Join us and make a difference when it matters most! At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.

Role and Responsibilities

The Manager will be accountable for the strategy and management of all systems and data within the regulatory affairs function. You will be responsible for the strategy and oversight of the regulatory information management system (RIM) and oversight of the regulatory systems support group and regulatory submission management and publishing teams. You will also be responsible for regulatory data management and also management of training and SOPs for regulatory. This role is also responsible for managing, developing and enhancing regulatory data management to ensure compliance, and to drive compliance and efficiencies in our regulatory processes using Veeva Vault RIM system.

Working in a highly collaborative environment this role will engage with multiple areas of the business.

Strategic oversight of the regulatory information management system

Responsible for the ongoing strategy of the regulatory information management system

Oversee the implementation, maintenance and optimization of Veeva RIM

Identify opportunities to enhance RIM capabilities to streamline regulatory processes.

Collaborate with various stakeholders across the business to integrate RIM across the business.

Liaising with vendor(s) and Mundipharma IT to ensure that Veeva delivers optimally for the business, evaluating Veeva functionality and upgrades and impact on the business and its data.

Monitor changes in regulatory and industry requirements and assess the impact of those on RIM requirements.

Regulatory Data ownership and reporting to the organization

Develop reporting mechanisms to ensure that senior management have oversight of compliance and risks.

Utilize data analytics and reporting tools to track compliance metrics and generate actionable insights to senior management.

Advise on the optimal use of regulatory data and create dashboards, reports etc. for internal and external audiences using business analytics reporting tools.

Conduct audits and assessments to ensure regulatory data compliance.

Responsible for Data maintained in external systems such as SPOR and the processes associated to maintaining the data.

Responsible for RA hard copy data management globally

Training and Process Development

Set up and/or update regulatory affairs SOPs, instructions, and guides for the use of Veeva and for other RIM activities.

Deliver appropriate training for users, both internally and for external vendors.

Management of submission management and publishing teams

Oversight of the external submission management activities.

Evaluate new technologies for future enhancements and improvements and lead any plans for implementation.

Responsible for assessing budget requirements around regulatory data management requirements.

What you’ll bring

Proven experience working in the pharmaceutical industry in a regulatory/regulatory operations function.

Proficiency in using Veeva Vault RIM and experience in driving its implementation and enhancement

Understanding global regulatory requirements and compliance standards

Understanding the importance of regulatory data management

Able to act independently and proactively problem solve.

Excellent written and verbal communication skills.

Ability to work in a fast-paced, dynamic environment.

What we offer in return

• Flexible benefits package
• Opportunities for learning & development through our varied programme
• Collaborative, inclusive work environment

Diversity and inclusion Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn’t just the right thing, but also the smart thing to do. We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness. We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect.

About Mundipharma

Mundipharma is a global healthcare company focussing on customers across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of pain management, infectious disease as well as other severe and debilitating disease areas. Their guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything they do. For more information visit www.mundipharma.com.

For more information about Mundipharma's guiding principles and commitment to diversity and inclusion visit: www.mundipharma.com/people