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Junior Regulatory Associate

2-5 years
Not Disclosed
10 May 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Junior Regulatory Associate


Job Summary

We are looking for a Junior Regulatory Associate to join our expanding team. The successful candidate will support global regulatory submissions and product life cycle activities, coordinate with cross-functional teams, and ensure high-quality regulatory documentation for pipeline and commercial products.


Key Responsibilities

  • Review and finalize global regulatory strategy documents and CTD sections for IND, CTA, BLA, NDA, and ANDA submissions

  • Coordinate with cross-functional teams, sites, and global Regulatory Affairs teams to author, review, and finalize high-quality regulatory dossiers

  • Prepare regulatory submissions to support pipeline molecule development and product launches

  • Monitor and manage timelines for MA transfers, variations, license renewals, supplements, and other product life cycle activities (e.g., annual reports, safety filings)

  • Collaborate with global and regional regulatory teams to prepare and submit documentation in compliance with international standards

  • Review and coordinate responses to Health Authority queries

  • Support responses to deficiency letters and regulatory feedback to ensure timely approvals

  • Participate in technical review meetings and provide regulatory advice

  • Identify regulatory risks on assigned projects and communicate them proactively for mitigation

  • Communicate project issues and outcomes effectively to global regulatory management and teams

  • Stay current on international legislation, regulatory guidelines, and market-specific practices

  • Manage and support regulatory inspections

  • Interpret and apply current regulations and guidance for assigned projects

  • Ensure adherence to client submission standards, policies, and procedures


Desirable Skills and Experience

  • 2–5 years of experience in a regulated life sciences environment

  • Hands-on experience in regulatory submissions, including CMC writing and labeling document management

  • Understanding of regulatory implications of product strategy and label development

  • Ability to interpret and apply regional/local regulatory guidance for CMC and safety submissions

  • Experience supporting both pre-approval and post-approval (maintenance) regulatory activities

  • Strong interpersonal and cross-cultural communication skills

  • In-depth knowledge of global and regional regulatory requirements

  • Strong analytical thinking and writing skills essential for regulatory documentation