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:
👉 Never Miss a Pharma Job Again
💼 Join our LIVE WhatsApp Group & Get Instant Updates. 📢 Click below to join:
📱 Join Click HereTo apply for this job please visit jobs.parexel.com.
📢 Join Our Social Channels
Join our WhatsApp and Telegram channels for the latest updates.
WhatsApp TelegramClick here to dismiss this popup for today.