The role includes in preparing, reviewing, and maintaining regulatory documentation for clinical development projects, ensuring alignment with applicable regulatory requirements and company standards. The role involves supporting regulatory submissions and maintaining records, tracking timelines, and coordinating with internal teams to gather data and information needed for regulatory filings. The Junior Associate will help monitor evolving regulations and guidelines, contribute to compliance activities, and support communication with regulatory authorities and external partners as directed. Routine tasks may include document formatting, data checking, organizing files, and providing administrative support to the Regulatory Affairs team.

Qualifications
Ability to work with Regulatory Documentation and support preparation, review, and organization of regulatory records.
Understanding of Regulatory Requirements and Regulatory Compliance relevant to clinical development and medical products.




Exposure to Regulatory Submissions and Regulatory Affairs processes, including basic knowledge of submission formats and timelines.
Strong attention to detail, accuracy in documentation, and ability to follow structured procedures and guidelines.
Effective written and verbal communication skills in English, with the ability to summarize technical information clearly.
Proficiency in standard office software (e.g., Word, Excel, PowerPoint) and comfort working with digital document management systems.
Ability to work collaboratively in cross-functional teams and manage multiple tasks with guidance in a rapid-paced environment.
Bachelor’s degree in pharmacy, life sciences, biotechnology, or a related field; prior internship or academic exposure to regulatory affairs or clinical research is an advantage.

📌 Junior Associate, Regulatory Affairs (New Delhi)
🏢 Intrinseque Health
📍 New Delhi