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Manager - Regulatory Affairs

Jubilant Pharmova
Jubilant Pharmova
10-12 years
Not Disclosed
Noida, India
10 Feb. 13, 2026
Job Description
Job Type: Full Time 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

Job Title: Manager – Regulatory Affairs

Location: India (based out of India, supporting Canada operations)

Employment Type: Full-Time

Job Category: Regulatory Affairs | Clinical Program Support | Global Regulatory Compliance

Experience Required: 10–12 years of industrial experience, with a minimum of 5 years in regulatory affairs for clinical programs


Job Context

The Manager – Regulatory Affairs will support MIBG I-131 clinical programs and other innovative products in the JDI pipeline. Reporting to the Director of Regulatory Affairs, the role involves developing and executing regulatory strategies for clinical programs, marketing applications in the US and Canada, and post-marketing activities.

This position requires global coordination with regulatory teams, clinical sites, and cross-functional stakeholders while ensuring compliance with regulatory requirements.


Key Responsibilities

Regulatory Support

  • Lead regulatory due diligence for product in-licensing or acquisitions, including products in clinical development or already approved

  • Re-evaluate regulatory strategies following major changes in formulation, clinical protocols, or marketing plans

  • Participate in meetings with regulatory agencies during pre-submission, NDA/NDS review, and post-approval phases

  • Prepare, review, and submit USFDA Investigational New Drug (IND) applications and Health Canada Clinical Trial Applications (CTA)

  • Manage filings for new protocol applications, protocol amendments, informed consent forms, clinical summary reports, regulatory correspondences, deviations, safety reports, cost recovery applications, exemptions, and CMC amendments

Key Interfaces

  • External: Regulatory agencies including USFDA and Health Canada

  • Internal: Clinical sites, Quality, Marketing, Clinical, Technical Services, and R&D departments


Education & Qualifications

  • Bachelor’s degree in Biology, Biochemistry, or related Life Sciences field

  • Desired certifications in Regulatory Affairs or Clinical Research preferred


Required Experience

  • 10–12 years of industrial experience, including 8 years post-highest qualification

  • Minimum of 5 years of hands-on experience in regulatory affairs supporting clinical programs and marketing applications


Skills Required

Functional Skills

  • Detail-oriented with strong organizational, analytical, and problem-solving capabilities

  • Functional expertise in global regulatory processes and submission requirements

Behavioral Skills

  • Self-motivated and capable of managing multiple projects in a fast-paced, cross-functional environment

  • Excellent communication and stakeholder management skills