Associate Director - IDMP

MSD; City Of London; On-site; GBP 50,000 - 70,000; Full time

Job summary

A Global Pharmaceutical Company in London seeks a Business Analyst to lead the implementation of IDMP standards. The successful candidate will manage regulatory data, contribute to IDMP strategy development, and ensure compliance with European authorities. Ideal candidates should have a background in regulatory affairs with proven leadership skills and the ability to manage cross-functional projects effectively.

Qualifications

• Comprehensive experience in Regulatory Affairs or Regulatory Operations.
• Practical knowledge and experience with ISO IDMP or IDMP/SPOR.
• Ability to lead by influence and work effectively in matrix organisational structures.

Responsibilities

• Lead the Data Governance body for internal data and systems.
• Contribute to the development of the IDMP strategy across the Company.
• Monitor non-EU IDMP-related activities.

Skills

Accountability

Adaptability

Communication

Project Management

Regulatory Affairs

Education

Bachelor’s degree in a science or information technology discipline

Job description

Job Description

The Identification of Medicinal Products (IDMP) Business Analyst will play a key role in the management and leadership of the European implementation of the ISO Identification IDMP’s standard in our Company. You will be part of a team progressing the strategic, project and operational activities in relation with regulatory data submitted to European authorities, including IDMP/SPOR (European implementation of ISO IDMP), DADI (replacement of the PDF electronic Application Form) and knowledge of XEVMPD ((Extended EudraVigilance Medicinal Product Dictionary, or Article 57) is necessary to properly transition to IDMP from strategic and tactical perspectives. You are also expected to cover several non-EU related topics.

Primary Activities

• XEVMPD

  • Participate, as required, to the internal activities associated with the use of XEVMPD data in the EMEA

  • Apply the knowledge of the data requirements and process to the transition to IDMP

• IDMP

  • Contribute to the development of the IDMP strategy in our Company. Working with peers across the Company to explain the strategy and integrate the needs and requirements from partner functions across Regulatory and other parts of the company

  • Contribute to the various projects to implement the IDMP strategy in our Company

  • Working with the Business System Owner and IT counterparts and in line with the System Development Life Cycle principles

  • Contribute to the setup and configuration of the IDMP Maintenance and Submission Tool, ensure the proper upload of IDMP data into the tool, define maintenance and submission processes with key stakeholders, and support the roll‑out of operational activities

  • Lead the Data Governance body where cross‑functional stakeholders contribute to evolve internal data and systems to converge in line with ISO IDMP and other internal use cases

  • Contribute to the evolution of the internal Regulatory Data Hub to ensure alignment with ISO IDMP concepts in line with the IDMP developments

  • Ensure synergies with IDMP related topics including XEVMPD and the Digital Application Dataset Integration.

  • Monitor non‑EU IDMP‑related activities

  • Report to the XEVMPD‑IDMP Team Lead and Senior Management on the progress of the IDMP program and projects

• External Activities

  • As the opportunity arises, represent our Company in European Industry Trade Association committees and meeting groups associated with IDMP. Taking on leadership roles within the Trade Association committees and represent the industry in meetings and negotiations with health authorities and other stakeholders

Qualifications, Skills & Experience

• Bachelor’s degree in a science or information technology discipline required

• Comprehensive experience in Regulatory Affairs or Regulatory Operations

• Practical knowledge and experience with ISO IDMP or IDMP/SPOR

• Good understanding of System Development Life Cycle methodology and the requirements for the validation of information management systems

• Demonstrated understanding of drug development and execution of regulatory program strategies within the countries and how this impacts regulatory information management strategies

• Experience as a leader on cross functional teams able to influence and motivate team members and Senior Management leading to high quality and on‑time delivery of project objectives

• Demonstrated situational leadership and creative problem solving within organizations and teams

• Ability to prioritize their own work across several ongoing projects

• Ability to lead by influence and work effectively in matrix organisational structures

• Ability to understand details but keep overall big picture view of projects

Required Skills: Accountability, Adaptability, Business Processes, Change Management, Clinical Trial Agreements (CTA), Clinical Trials, Communication, Cross‑Cultural Awareness, Data Management, Employee Training Programs, FDA Regulations, Global Health, Internal Processes, Management Process, Mentorship, Pharmacovigilance, Policy Implementation, Project Management, Regulatory Affairs Management, Regulatory Compliance, Regulatory Labeling, Regulatory Operations, Regulatory Submissions, Stakeholder Management plus 4 more.

Preferred Skills:

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Current Contingent Workers apply HERE

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Employee Status: Regular

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Flexible Work Arrangements: Hybrid

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Job Posting End Date: 11/10/2025

Requisition ID: R371363

Job posting is effective until 11:59:59PM on the day before the listed job posting end date. Please ensure you apply to a job posting no later than the day before the job posting end date.