Senior IDMP Consultant

I am currently supporting a Global Regulatory Affairs Consultancy in the search for a Senior IDMP Consultant on a freelance basis. My Client is offering a full FTE for up to 12 months. This opportunity is able to be worked remotely, however may require onsite work once a month in Germany.

IDMP Consultant responsibilities include, but not limited to:

• Provide consulting and implementation support for IDMP projects
• Help define the requirements for IDMP data Collection, Compilation and Migration strategy
• Help define the overall business strategy and plan for executing IDMP submissions
• Define the process for maintaining data in Data collection repository, including XEVMPD related data changes, and updates to IDMP data
• Work directly with different stakeholders like local country SPOC (Single Point of Contact), business SPOC from RA, PV, RIMS, R&D, GMS (Global Medical Safety), Marketing, Labeling etc. and any third party vendors to procure IDMP data and for managing changes to existing data in Data Collection Repository
• Author detailed IDMP Process SOPs, work instructions, manuals, training guides with contribution from other stakeholders
• Analyse and prepare a plan for implementation of IDMP guidelines
• Be a business analyst and subject matter expert to identify and document RIM related user requirements and use cases in collaboration with cross-functional stakeholders
• Develop procedure documents or best practices for RIM, implementing and managing RIM governance
• Monitor, analyze and track new functionality of new RIM releases and implement in collaboration with GIS, vendors and cross-functional key business stakeholders
• Assist in audit and inspection activities including retrieval of Regulatory Information

 Suitable candidates will have experience in:

• Regulatory Information Management
• XEVMPD
• IDMP knowledge
• Industry RIMS applications experience (e.g. Aris Register, Liquent Insight, CuneRIM etc.)

Full job description available upon application.

I specialise in recruiting Regulatory Affairs professionals throughout Europe, if you would like to speak to me regarding the above position then please call me today on +44 (0)1293 77 66 44 for a confidential discussion.

Alternatively you can reach me on Linked In or e-mail me on JASmith@barringtonjames.com.

If you are interested in discussing any of my other vacancies, or simply want to be made aware of opportunities as they arise then please contact me or have a look at available jobs on the Barrington James Website.

I look forward to hearing from you soon!

Jasmine Smith

Contract Consultant ~ Regulatory Affairs

+ 44 (0)1293 77 66 44