Clinical Regulatory Affairs Specialist - Micro Labs Limited, Full-time Job

Job Requirements

We are looking for a Clinical Regulatory Affairs Specialist to join our team at Micro Labs Limited in Bangalore/Bengaluru. The successful candidate will be responsible for providing regulatory support to the clinical department and ensuring compliance with applicable regulations. The ideal candidate should have a strong background in regulatory affairs and experience in the pharmaceutical industry.

The Clinical Regulatory Affairs Specialist will be responsible for:

• Developing and implementing regulatory strategies for clinical trials

• Preparing and submitting regulatory documents to the relevant authorities

• Monitoring and tracking regulatory submissions

• Ensuring compliance with applicable regulations

• Liaising with internal and external stakeholders

• Providing regulatory advice and guidance

• Maintaining up-to-date knowledge of regulatory requirements