🌍 Looking for Pharma Jobs in India? Parexel Hiring Regulatory Affairs Professionals 🌍
💻 Remote Role | 📍 Bengaluru | 🚀 Global Exposure | 📈 Strong Career Growth
Parexel is a globally recognized clinical research organization (CRO) that provides end-to-end solutions in clinical development, regulatory consulting, and market access.
🧬 The company is known for its innovation-driven approach and strong commitment to improving global healthcare outcomes.
🌐 With a presence across multiple countries, Parexel ensures high standards of regulatory compliance and scientific excellence. The company collaborates with pharmaceutical, biotechnology, and medical device companies to bring life-saving therapies to patients worldwide.
💼 Job Details
- 🏢 Company Name: Parexel
- 📍 Location: Bengaluru (Remote)
- 💻 Work Type: Remote
📋 Job Description
Parexel is hiring for a Regulatory Affairs role focused on CMC submissions, regulatory documentation, and global compliance.
🎯 This position plays a critical role in ensuring successful regulatory submissions and coordination across teams.
Senior Regulatory Affairs Associate
- 📑 Department: Regulatory Affairs
- 🌐 Market: Global (US & Canada focus)
- 📝 Role: CMC documentation, submission planning, and regulatory coordination
🛠️ Skills/Qualifications
- 📋 Strong knowledge of regulatory affairs and CMC documentation
- 🌍 Understanding of global regulatory guidelines (US & Canada)
- 💻 Experience with eCTD submissions and regulatory systems
- 🤝 Excellent communication and coordination skills
- 🔍 Attention to detail and documentation accuracy
- 🌐 Ability to work cross-functionally with global teams
📝 Key Responsibilities
- 📊 Compile annual reportable and approved CMC changes
- 📑 Prepare CMC Submission Content Plan (SCP)
- ✍️ Author Module 1 regulatory documents
- 🤝 Coordinate with regulatory and operations teams
- 💻 Ensure proper eCTD submission formatting
- 📈 Track submissions and regulatory acknowledgements
- 🗂️ Maintain regulatory documentation in repository systems
- ✅ Close regulatory events in RIM systems
🎁 Benefits/Perks
- 🏠 Remote work flexibility
- 🌍 Global exposure in regulatory affairs
- 📈 Career growth in pharma and CRO industry
- 📚 Learning and development opportunities
- 🤝 Collaborative and inclusive work culture
📧 How to Apply
Interested candidates can apply directly through the official careers page:
🔗 Parexel Careers Portal (Search Job ID: R0000040066)
Verified Post: To confirm the legitimacy of this posting, you can view the original announcement on the Parexel Careers page.
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Apply now to join a globally recognized CRO and advance your career in regulatory affairs.
🌟 Why You Should Join
Parexel offers a strong work culture focused on innovation, empathy, and global impact.
💊 Employees work on meaningful projects that directly contribute to patient health outcomes.
🚀 The company provides long-term career stability and continuous learning opportunities.
❓ FAQs
Who can apply for this role?
A: Candidates with experience in regulatory affairs, CMC, or clinical research can apply.
Is this a remote job?
A: Yes, this is a remote role based in Bengaluru.
What is the job focus?
A: The role focuses on regulatory submissions, CMC documentation, and compliance.
Are there growth opportunities?
A: Yes, Parexel offers strong career growth and global exposure in regulatory affairs.
Join Parexel – Lead Global Regulatory Submissions from Home!
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