Clinical Regulatory Affairs Specialist - Micro Lab

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