Looking for pharma jobs in India? Parexel is hiring Regulatory Affairs professionals for remote roles with global exposure and strong career growth opportunities.
Contents
About the Company
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 critic al 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
Verification: 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?
Candidates with experience in regulatory affairs, CMC, or clinical research can apply.
Is this a remote job?
Yes, this is a remote role based in Bengaluru.
What is the job focus?
The role focuses on regulatory submissions, CMC documentation, and compliance.
Are there growth opportunities?
Yes, Parexel offers strong career growth and global exposure in regulatory affairs.
