Parexel Work from home Hiring Regulatory Affairs Consultant

Parexel Work from Home Hiring Regulatory Affairs Consultant

Join Parexel as a Regulatory Affairs Consultant – Work Remotely in India

Are you an experienced Regulatory Affairs professional looking for a flexible remote job? Parexel, a leading global clinical research organization, is hiring a Regulatory Affairs Consultant to support regulatory strategies and compliance processes for biopharmaceutical and medical device companies. This work-from-home opportunity offers a chance to collaborate with industry leaders and contribute to global regulatory initiatives.

About Parexel

Parexel is a globally recognized clinical research organization (CRO) specializing in regulatory affairs, clinical trials, and pharmaceutical consulting. With a strong commitment to innovation, patient safety, and regulatory excellence, Parexel helps pharmaceutical companies bring their products to market efficiently and in compliance with global regulations.

Regulatory Affairs Consultant – Job Overview

Current Vacancies in Department:

• Regulatory Affairs – Labeling and Safety Compliance

Job Location:

• Remote – Work from Home (India)

Required Education:

• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field

Experience Required:

• Minimum 5 years of experience in Regulatory Affairs
• Expertise in safety labeling changes, CCDS (Company Core Data Sheet) creation or updates, and change control assessments
• Prior experience with Centralized Products is a plus
• Proficiency in Veeva RIMS and TVT Tool is preferred

Key Responsibilities

• Manage safety labeling changes impacting Product Information
• Create and update Company Core Data Sheets (CCDS)
• Conduct regulatory impact assessments for product modifications
• Oversee change control processes in compliance with regulatory requirements
• Work collaboratively with cross-functional teams, ensuring timely and efficient regulatory submissions
• Maintain up-to-date knowledge of EU, UK, CH, AU, and NZ regulatory frameworks

Skills & Qualifications Needed

•  Strong understanding of global regulatory requirements
• Experience handling safety labeling changes
• Knowledge of Centralized Products regulations
• Proficiency in Veeva RIMS & TVT Tool
• Excellent communication and problem-solving skills

How to Apply?

Don’t miss this opportunity to work with Parexel, a leading name in regulatory affairs consulting. If you meet the above qualifications, apply now using the link below:

🔗 Apply Here

Tagged as: Global Pharma Jobs, Pharmaceutical Careers, Pharmaceutical Jobs