ClinChoice is hiring for a Senior Associate – Regulatory Affairs role in Bengaluru, India. This opportunity is ideal for life sciences and pharmacy professionals with 3–5 years of experience who are interested in Regulatory Affairs, Regulatory Publishing, eCTD submissions, and electronic submission management.

Job Overview

About ClinChoice

ClinChoice is a global clinical research and professional services organization supporting pharmaceutical, medical device, vaccine, and consumer healthcare innovators. Established in 1995, the company provides expertise across clinical operations, biometrics, regulatory affairs, pharmacovigilance, quality services, medical affairs, toxicology, and technology solutions.

With a global delivery network across multiple countries, ClinChoice supports organizations in maintaining regulatory compliance and advancing healthcare products.

Job Summary

ClinChoice is seeking a Senior Associate – Regulatory Affairs to support electronic regulatory submissions and regulatory publishing activities.

The role involves preparing, formatting, validating, and compiling submission-ready documents in accordance with global health authority requirements. Candidates will support eCTD and non-eCTD submissions, perform technical validation, maintain submission documentation, and coordinate with internal teams to ensure submission readiness.

This is an excellent opportunity for professionals looking to build or expand their careers in Regulatory Affairs, Regulatory Operations, and Regulatory Publishing within the pharmaceutical and life sciences industry.

Key Responsibilities

As a Senior Associate – Regulatory Affairs, you will be responsible for:

• Supporting the preparation of eCTD and non-eCTD regulatory submissions
• Formatting regulatory documents according to submission requirements
• Performing hyperlinking, bookmarking, and PDF optimization
• Assisting with regulatory submission compilation and publishing activities
• Conducting technical validation checks before submission
• Maintaining submission trackers and documentation logs
• Ensuring metadata accuracy and correct document placement
• Supporting submission lifecycle management activities
• Managing new, replace, and delete submission sequences
• Coordinating with internal teams to ensure submission readiness
• Supporting compliance with global health authority requirements

Required Qualifications

Candidates applying for this Regulatory Affairs job in Bengaluru should have:

• A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline
• 3–5 years of relevant professional experience
• Good knowledge of Microsoft Office, including Word, Excel, and PowerPoint
• Strong attention to detail and documentation skills
• Good written and verbal communication abilities
• Effective time management skills
• Ability to work collaboratively with cross-functional teams

A basic understanding of the pharmaceutical regulatory environment is preferred but may not be mandatory.

Preferred Skills

Candidates with exposure to the following areas may have an advantage:

• eCTD publishing concepts
• Regulatory publishing and submission management
• Electronic regulatory submissions
• Submission lifecycle management
• Veeva Vault
• Lorenz DocuBridge
• Other eCTD publishing tools
• Regulatory Operations
• Document formatting and PDF optimization
• Metadata management and technical validation

Why Consider This Regulatory Affairs Opportunity?

This position offers an opportunity to work in the growing field of Regulatory Publishing and Regulatory Operations. Regulatory professionals play an important role in ensuring that pharmaceutical and life sciences companies prepare accurate, compliant, and technically valid submissions for health authorities.

Candidates can gain exposure to:

• Global regulatory submission processes
• eCTD publishing workflows
• Regulatory Operations
• Electronic document management
• Submission lifecycle management
• Publishing and validation tools
• Cross-functional pharmaceutical industry collaboration

Who Should Apply?

This ClinChoice Regulatory Affairs job may be suitable for:

• Regulatory Affairs professionals with 3–5 years of experience
• Regulatory Publishing Associates
• Regulatory Operations professionals
• Pharmacy graduates interested in regulatory submissions
• Life Sciences professionals with publishing experience
• Candidates with exposure to eCTD, Veeva Vault, or Lorenz DocuBridge

Salary and Compensation

The expected salary for a Senior Associate – Regulatory Affairs in Bengaluru may vary based on experience, technical skills, current compensation, and the final selection process.

Estimated salary range: ₹6,00,000 – ₹10,00,000 per year (CTC).

Actual compensation will be determined by ClinChoice based on the candidate’s qualifications and experience.

How to Apply

Application Link