0 years
0 Lacs
Posted:6 days ago|
Platform:
On-site
Full Time
Contract: Permanent Full-Time
Closing Date: 05/12/25
We are seeking a Global Regulatory Data Standards Expert to lead the implementation and governance of ISO IDMP standards and ensure ongoing compliance with EMA requirements for structured medicinal product data. This role will also oversee XEVMPD submissions and support the transition to IDMP, playing a critical part in global regulatory data management.
Key Responsibilities:
Required Skills & Experience:
Why Join G&L?:
This role offers the opportunity to work at the forefront of global drug development while embedded with a top-tier pharmaceutical client. You will gain exposure to high-impact projects, contribute to advancing innovative therapies, and play a strategic role in shaping regulatory pathways worldwide - all while being supported by our expert, global teams of consultants.
If you're passionate about regulatory excellence and digital transformation in life sciences, we’d love to hear from you.
If you would be interested in joining the team at G&L Scientific, please send your CV to [email protected] today.
G&L Scientific is an equal opportunities employer and welcomes applicants from all sections of the community regardless of their gender, religious belief, political opinion, sexual orientation, disability, age, marital status or race.
We recruit based on talent alone and firmly believe that an individual’s background should play no part in the recruitment and selection process.
G&L Healthcare Advisors
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