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Senior Regulatory Affairs Associate

Parexel
Parexel
0-2 years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 Affairs Associate

Primary Location: India (Remote)
Category: Regulatory Affairs / Pharmaceuticals
Job Type: Full-Time


About Parexel

At Parexel Consulting, we help biopharmaceutical and medical device companies navigate the complex and evolving regulatory landscape. By combining scientific, technical, and regulatory expertise, our team enables clients to bring innovative products to market faster while ensuring compliance and lifecycle management.

Join Parexel to work on global projects, collaborate with diverse clients, and advance your career with mentorship, challenging assignments, and a flexible remote work environment.


Role Overview

The Senior Regulatory Affairs Associate will manage regulatory submissions, lifecycle management, and compliance activities for a variety of products, including biologicals, vaccines, recombinant proteins, monoclonal antibodies, plasma-derived products, and small molecules. You will operate across key global markets such as the US, EU, Japan, Canada, Switzerland, and Australia, ensuring regulatory strategies align with regional and global requirements.


Key Responsibilities

  • Lead and contribute to new product registrations, lifecycle management, and renewal submissions for multiple markets.

  • Prepare, review, and author Marketing Authorization Applications (MAAs), variations, and other regulatory documents for global filing.

  • Ensure regulatory submissions comply with regional and international frameworks, including US FDA, EMA, PMDA (Japan), Health Canada, TGA (Australia), and Swissmedic.

  • Maintain a strong understanding of global pharmaceutical legislation and guidance, particularly related to regulatory CMC requirements.

  • Provide strategic input on regulatory pathways, submission strategies, and compliance risk mitigation.

  • Collaborate with cross-functional teams and external stakeholders to facilitate timely submission and approvals.

  • Mentor junior regulatory associates, support knowledge sharing, and promote best practices in regulatory operations.

  • Stay updated on regional trends and changes in regulatory frameworks to proactively adapt strategies.


Qualifications & Experience

  • Proven experience in global regulatory affairs, preferably with 5+ years handling biologics, vaccines, recombinant proteins, monoclonal antibodies, plasma-derived products, and small molecules.

  • Strong knowledge of regulatory frameworks across US, EU, Japan, Canada, Switzerland, and Australia.

  • Experience preparing and submitting MAAs, variations, and lifecycle management documents.

  • Excellent communication, collaboration, and interpersonal skills.

  • Ability to work independently while managing multiple global projects.

  • Strong understanding of CMC regulatory requirements in the ICH regions.


Why Join Parexel

  • Work on global, high-impact regulatory projects across multiple therapeutic areas.

  • Gain exposure to diverse regulatory frameworks and product types.

  • Enjoy flexible remote working with a supportive, innovative team.

  • Benefit from professional development, mentorship, and opportunities to enhance your regulatory expertise.


Remote Work Policy

This role is remote but requires collaboration with global teams, ensuring effective communication and timely submission of regulatory deliverables.