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Senior Regulatory Associate

3+ years
₹7.5 LPA – ₹10 LPA
10 July 22, 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

Senior Regulatory Associate – Publishing and Submissions
Location: [Not specified]
Experience Required: Experience in Publishing and Submissions is required
Job Type: Full-Time


Job Description:
We are currently seeking a Senior Regulatory Associate to join our Regulatory Operations team. This role involves the end-to-end management of regulatory submissions across multiple formats and markets, ensuring accuracy, compliance, and timely delivery. You will also support audits, mentor junior staff, and help strengthen internal processes to meet global regulatory standards.


Key Responsibilities:

Regulatory Submission & Document Publishing:

  • Prepare, publish, dispatch, and archive regulatory submissions in agency-approved formats (e.g., eCTD, NeeS, Paper).

  • Ensure high-quality, submission-ready documents by formatting, hyperlinking, and processing documents in MS Word and Adobe Acrobat.

  • Troubleshoot formatting or document issues and resolve any technical discrepancies.

Compliance & Audit Support:

  • Support regulatory audits and compliance activities, ensuring complete adherence to client-specific and internal processes.

  • Ensure all deliverables are accurate, validated, and submission-ready within established timelines.

Cross-functional Coordination:

  • Collaborate with cross-departmental teams (e.g., Regulatory Affairs, Clinical, CMC) for planning, preparation, and quality control checks.

  • Maintain up-to-date knowledge of regulatory guidelines, agency submission standards, and internal SOPs.

Tool Proficiency & Operational Oversight:

  • Operate various publishing and validation tools (e.g., pharmaREADY®, Lorenz, Extedo, eCTD Express, Veeva Vault, etc.).

  • Manage the technical aspects and provide status updates for assigned submissions.

Training & Process Improvement:

  • Train and mentor junior team members, ensuring consistency and knowledge-sharing.

  • Contribute to the revision of SOPs, work instructions, and training documents to maintain regulatory compliance and operational efficiency.


Desirable Skills and Experience:

  • Proven experience in Regulatory Publishing and Submissions.

  • Strong technical skills in eCTD publishing and validation tools.

  • Hands-on experience with Adobe Acrobat, MS Word, and formatting tools.

  • Sound understanding of global regulatory authority requirements (e.g., FDA, EMA, Health Canada).

  • Excellent coordination, documentation, and communication skills.

  • Prior experience in mentoring or training junior team members is highly desirable.


Estimated Salary: ₹7.5 LPA – ₹10 LPA (based on experience and tool proficiency)