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Regulatory Affairs Manager

8+ years
Not Disclosed
10 Nov. 14, 2025
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

Regulatory Affairs Manager 

Job Title

Regulatory Affairs Manager

Location

Bengaluru, India (Home-based option available)

Job ID

R1510705

Employment Type

Full-time


Job Overview

An individual contributor role requiring advanced regulatory knowledge gained through several years of experience. Works independently with limited supervision and handles complex regulatory projects, technical writing, client interactions, and cross-functional collaboration.


Key Responsibilities

1. Regulatory Project Leadership

  • Serve as Regulatory Team Leader for complex projects.

  • Act as Project Manager for standalone regulatory projects as needed.

  • Lead regulatory strategies, discussions, and communication with clients and agencies.

2. Technical Writing & Documentation

  • Write high-quality regulatory and technical documents with minimal oversight.

  • Review and manage regulatory submissions and project deliverables.

  • Contribute to drafting or reviewing regulatory SOPs.

3. Client & Stakeholder Management

  • Build strong relationships with multiple clients.

  • Attend client meetings independently to discuss regulatory issues.

  • Present regulatory deliverables at bid defense meetings (phone/in-person).

4. Budget & Revenue Oversight

  • Review and manage project budgets, including out-of-scope activities.

  • Ensure revenue recognition and escalate concerns appropriately.

5. Mentoring & Training

  • Provide guidance and feedback to junior colleagues.

  • Support training and development initiatives.

6. Regulatory Agency Interactions

  • Manage meetings with global and regional Regulatory Authorities.

  • Support global, regional, or cross-functional regulatory initiatives.

7. Process & Quality Improvement

  • Recommend enhancements in processes, systems, and SOPs.

  • Participate in organizational or IQVIA-led regulatory initiatives.

8. Other Responsibilities

  • Perform additional tasks delegated by regulatory management.

  • Serve as reviewer/approver for cross-functional SOPs.

  • Support marketing authorization transfers (MAT), publishing, and submission strategies.


Qualifications

Education

  • Bachelor’s or Master’s degree in Life Sciences or related discipline (required).

Experience

  • Minimum 8 years of relevant regulatory affairs experience.

  • Strong understanding of:

    • R&D processes (CMC, Preclinical, Clinical)

    • Regional regulatory procedures

    • Marketing authorization transfers

    • Pharmacovigilance requirements related to MAT

Technical Skills

  • Expertise in regulatory strategy, timelines, and documentation requirements.

  • Strong understanding of regulatory intelligence in the relevant region.

  • Proficiency in Microsoft Office and regulatory publishing tools.

Soft Skills

  • Strong analytical and organizational skills.

  • Ability to work independently on multiple projects.

  • Ability to build strong cross-functional and client relationships.

  • Adaptability to rapidly changing regulatory environments.

Certifications

  • Relevant regulatory certifications (as required by region/country).


Key Competencies

  • Advanced regulatory knowledge

  • Project leadership

  • Decision-making under supervision

  • Process improvement mindset

  • Effective communication and stakeholder engagement