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Regulatory Affairs Consultant

Parexel
Parexel
6+ years
preferred by company
10 Feb. 6, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Regulatory Affairs Consultant
Location: India (Remote)
Employment Type: Full-Time
Experience Required: 6+ Years


Job Overview

Parexel is seeking an experienced Regulatory Affairs Consultant to join its global consulting team. This role offers the opportunity to work remotely from India while supporting biopharmaceutical and medical device companies in navigating complex global regulatory environments.

As part of Parexel Consulting, you will leverage your scientific, technical, and regulatory expertise to design and execute effective regulatory strategies that accelerate product approvals and support lifecycle management across international markets. This position provides broad exposure to multiple therapeutic areas, product types, and global regulatory frameworks, supported by a collaborative culture and ongoing professional development.


Key Responsibilities

  • Lead and support global and regional regulatory strategies for biologics, vaccines, recombinant proteins, monoclonal antibodies, plasma-derived products, and small molecules.

  • Manage new registrations, lifecycle management activities, and renewals across major regulatory markets including the US, EU, Japan, Canada, Switzerland, and Australia.

  • Prepare, author, and review regulatory submission dossiers, including Marketing Authorization Applications (MAAs) and post-approval variations.

  • Contribute to the planning, coordination, and delivery of regulatory submissions in alignment with global and regional regulatory requirements.

  • Provide regulatory guidance on Chemistry, Manufacturing, and Controls (CMC) aspects in accordance with ICH guidelines and regional regulations.

  • Monitor and interpret evolving global regulatory legislation, guidelines, and regional trends to ensure compliance and strategic alignment.

  • Collaborate closely with internal cross-functional teams and external clients, delivering high-quality regulatory solutions independently and efficiently.


Required Qualifications and Experience

  • Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotechnology, Chemistry, or a related scientific discipline.

  • Minimum 6 years of hands-on regulatory affairs experience, with a strong focus on global submissions and lifecycle management.

  • Proven experience handling regulatory activities for biologics, vaccines, and small molecules across multiple international markets.

  • Strong knowledge of global regulatory frameworks, submission pathways, and pharmaceutical legislation, particularly within ICH regions.

  • Demonstrated expertise in regulatory CMC requirements.

  • Excellent written and verbal communication skills with the ability to work independently in a remote environment.

  • Strong attention to detail, problem-solving ability, and strategic mindset.


Why Join Parexel

Parexel is a global leader in biopharmaceutical services, known for its scientific excellence and patient-first approach. Consultants at Parexel work in a flexible, collaborative environment that values innovation, integrity, and continuous learning. You will gain exposure to diverse clients and products while advancing your regulatory career with the support of experienced mentors and global teams.


About Parexel

Parexel partners with biopharmaceutical and medical device companies worldwide to help bring innovative therapies to patients faster. With deep regulatory, clinical, and scientific expertise, Parexel supports products across the entire development lifecycle.


Apply now on ThePharmaDaily.com to advance your career in global regulatory affairs with a leading life sciences consulting organization.