Job Description
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Regulatory Submissions Manager in India.
This role is a key leadership position within regulatory affairs, focused on driving end-to-end regulatory submissions across global drug development programs. You will oversee critical filings such as CTA, IND, and MAA while ensuring compliance with evolving global regulatory standards. The position plays an important role in enabling timely development and approval of new therapies by providing strategic regulatory guidance and operational execution support. You will collaborate closely with cross-functional teams including clinical, medical, and development stakeholders to ensure high-quality submissions. The role requires strong ownership of regulatory processes, with the ability to operate independently while contributing to broader best practices. This is a highly impactful environment where precision, scientific understanding, and regulatory expertise directly influence patient access to innovative treatments.
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Regulatory Submissions Manager in India.
This role is a key leadership position within regulatory affairs, focused on driving end-to-end regulatory submissions across global drug development programs. You will oversee critical filings such as CTA, IND, and MAA while ensuring compliance with evolving global regulatory standards. The position plays an important role in enabling timely development and approval of new therapies by providing strategic regulatory guidance and operational execution support. You will collaborate closely with cross-functional teams including clinical, medical, and development stakeholders to ensure high-quality submissions. The role requires strong ownership of regulatory processes, with the ability to operate independently while contributing to broader best practices. This is a highly impactful environment where precision, scientific understanding, and regulatory expertise directly influence patient access to innovative treatments.
