Senior Regulatory Affairs Associate

Parexel International; India; On-site; INR 900,000 - 1,200,000; Full time

Job summary

A global clinical research organization is seeking a Senior Regulatory Affairs Associate in India. This role involves managing the regulatory lifecycle for products, supporting local and global teams, ensuring compliance with national regulations, and preparing documentation for audits and submissions. Ideal candidates should have 5 to 8 years of experience in regulatory affairs and a strong understanding of regulatory impact assessments. The position emphasizes collaboration across departments, ensuring timely closures of regulatory commitments.

Qualifications

• 5 to 8 years of experience in regulatory affairs.
• Strong understanding of the CTD/eCTD structure, especially Module 1.
• Ability to evaluate regulatory impact assessments.

Responsibilities

• Prepare, compile, and review country‑specific regulatory documentation.
• Coordinate and submit regulatory submissions including renewals and variations.
• Support the local RA representative during audits and inspections.

Skills

Strong knowledge of global regulatory guidelines

Experience in lifecycle management

Familiarity with change control processes

Good documentation skills

Ability to work effectively with cross-functional teams

Strong organizational skills

Prior experience with regulatory databases

Job description

Senior Regulatory Affairs Associate

The role is responsible for supporting end‑to‑end regulatory lifecycle management activities for assigned products in the local market. This includes preparation and maintenance of country‑specific regulatory documentation, coordination of post‑approval changes, and ensuring compliance with national regulatory requirements. The position also supports audits/inspections and collaborates with cross‑functional teams (Quality, Supply Chain, Pharmacovigilance, Medical, Commercial) to maintain regulatory compliance.

1. Preparation, Organization & Coordination of Local Regulatory Documentation

• Prepare, compile, and review country‑specific regulatory documentation (e.g., Module 1, administrative forms, declarations, national templates) in accordance with local health authority requirements.
• Support regulatory submissions including new registrations, renewals, variations, PSURs/PBRERs, safety updates, label updates, and CMC‑related changes.
• Maintain and update local regulatory databases (VEEVA RIMS), tracking systems, and product registration archives to ensure compliance with local legislation.
• Ensure that all documents meet formatting, quality, and content standards required for national submissions.
• Liaise with global/regional RA teams to obtain submission components and ensure alignment with global dossiers.

2. Provide Local Input for Post‑Approval Changes & Change Control

• Evaluate change control notifications related to manufacturing, quality, safety, or labelling changes and provide country‑specific regulatory impact assessments.
• Work with global/regional RA, Quality, and Supply Chain teams to ensure timely implementation of post‑approval changes as per national regulatory timelines.
• Prepare and submit variation dossiers or notifications based on local regulatory classifications and guidelines.
• Track approval timelines and ensure that all regulatory commitments arising from changes are fulfilled promptly.

3. Support in Audits, Inspections & Regulatory Compliance

• Support the local RA representative during internal audits, external audits, and health authority inspections.
• Coordinate and prepare documentation required for inspections, ensuring readiness of RA records and systems.
• Assist in responding to audit observations and regulatory findings.
• Collaborate with cross‑functional teams to ensure timely closure of Corrective and Preventive Actions (CAPAs).
• Ensure continuous compliance with evolving national regulations and proactively identify potential risks.

Key Skills & Competencies Required

• Strong knowledge of global regulatory guidelines and understanding of the CTD/eCTD structure, especially Module 1.
• Experience in lifecycle management: renewals, variations, PSUR/PBRER submissions, label updates, CMC changes.
• Familiarity with change control processes and regulatory impact assessments.
• Good documentation skills and attention to detail.
• Ability to work effectively with cross‑functional and global teams.
• Strong organizational, planning, and communication skills.
• Prior experience with regulatory databases or submission‑tracking tools is an advantage.

Experience Level:

5 to 8 years