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Regulatory Associate

0-2 years
Not Disclosed
10 Sept. 24, 2025
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

Job Title:

Regulatory Associate

Location:

Gurugram, Haryana, India

Company:

Syneos Health®

Job ID:

25101793


Position Overview:

Supports regulatory agency submissions, regulatory research, and product development. Prepares regulatory submission documents and product lifecycle maintenance materials under supervision, ensuring compliance with applicable regulations and guidelines.


Key Responsibilities:

  • Assist in preparation of product development documents, including gap analyses and clinical development plans.

  • Support preparation of regulatory submission documents for:

    • Investigational New Drug applications (INDs)

    • New Drug Applications / Marketing Applications (NDAs/MAAs)

    • Drug Master Files (DMFs)

    • Variations, renewals, marketing authorization transfers (MATs)

    • Other lifecycle maintenance activities.

  • Conduct regulatory research to identify precedents and support orphan drug designation requests.

  • Perform quality checks on regulatory documents.

  • Assist with submissions of other regulatory documents as required.

  • Gather, compile, analyze, and report regulatory information.

  • Maintain correspondence and information tracking across multiple projects.


Qualifications:

  • Bachelor’s degree in Science/Healthcare field, or equivalent combination of education and experience.

  • Excellent interpersonal and communication skills.

  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).

  • Strong analytical skills and attention to detail.

  • Good time and project management skills preferred.

  • Ability to work both independently and as part of a team.

  • Ability to work on multiple projects with varying instructions simultaneously.

  • Fluent in English (speaking, writing, reading).


Additional Information:

  • Tasks may evolve according to project requirements.

  • Syneos Health promotes diversity, inclusion, career development, and employee well-being.

  • This posting may represent a potential upcoming opportunity, and applicants may be added to the talent pipeline.


Summary:

Supports regulatory submissions, regulatory research, and product development. Creates submission documents for INDs, NDAs/MAAs, DMFs, variations, renewals, MATs, and other lifecycle maintenance activities under supervision. Ensures compliance with regulations and assists cross-functionally to deliver accurate regulatory materials.