Data Associate – Regulatory Information

About Us:

At Artixio, we support global pharmaceutical, biologics, and medical device companies in navigating complex regulatory landscapes. We are seeking a detail-oriented and driven Data Associate

Key Responsibilities:

• Collect, review, and organize regulatory data from public health authority sources (e.g., US FDA, EMA, CDSCO, HSA, TFDA, NPRA, etc.).
• Extract and compile information on product approvals, classifications, guidelines, and regulatory requirements across markets.
• Maintain and update regulatory databases, trackers, and internal documentation with a high degree of accuracy.
• Perform periodic audits and quality checks to ensure data completeness, consistency, and compliance.
• Support regulatory affairs team in preparing documentation, summaries, and reports for internal and client-facing projects.
• Monitor and log updates in regulatory procedures, timelines, and dossier requirements from official sources.

Required Skills & Qualifications:

• Bachelor’s degree in Pharmacy, Life Sciences, Regulatory Affairs, Public Health, or a related field.
• 1–3 years of experience in regulatory affairs, data entry/management, or scientific documentation. (Freshers with strong skills may also apply.)
• Strong organizational and analytical skills with high attention to detail.
• Familiarity with regulatory authorities and global submission processes is preferred.
• Proficiency in MS Excel, Google Sheets; ability to handle structured data.
• Strong written communication skills and documentation discipline.

Preferred Attributes:

• Interest in regulatory affairs, compliance, and document/data lifecycle management.
• Experience working with regulatory agency databases such as Drugs@FDA, EMA, or similar.