Job Description
Become a Part of ACCURIDS Join us and help shape the future of pharmaceutical data! At ACCURIDS, we’re building the data backbone behind life-science innovation — a system that identifies, links, and standardizes critical enterprise data in compliance with global standards such as ISO IDMP. We help global life-science companies launch products faster, more safely, and with better patient outcomes. At ACCURIDS, you’ll join a collaborative, growth-driven environment where your work makes a real impact from day one. How you’ll make an impact: You guide and advise global pharmaceutical customers on adopting ISO IDMP and other crucial data standards (such as ICH and GMP), helping them navigate how these global frameworks are adapted local, country-specific implementations. You evaluate and structure complex customer data modeling needs, translating chaotic real-world data into clear, standardized enterprise structures. You drive change management efforts at the enterprise level, steering customer organizations toward global standardization while balancing business expectations. You collaborate internally with the ACCURIDS services and product teams, translating customer insights, regulatory requirements and global standards into actionable inputs for our product roadmap. You track industry intelligence and participate in standardization initiatives, ensuring we anticipate major regulatory shifts and proactively build solutions to mitigate risks. What helps you succeed: You bring extensive pharmaceutical industry experience across regulatory, clinical, manufacturing, or R&D, giving you deep insight into core industry processes and structures. You have expert-level knowledge of ISO Standards, ICH Guidelines, and GMP requirements. You possess strong data-structuring capabilities , with a proven ability to collect, analyze, and model customer data needs. You are an exceptional communicator and presenter who can articulate complex technical solutions and influence both i
