This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Regulatory Affairs Associate based in India. This role offers the opportunity to support global clinical development programs by managing regulatory submissions and ensuring compliance across multiple regions.You will contribute to bringing innovative therapies closer to patients by coordinating critical regulatory activities throughout the clinical trial lifecycle.The position combines regulatory expertise, project management, and cross-functional collaboration within a global healthcare environment.You will work closely with international teams to deliver high-quality submissions while managing timelines, risks, and regulatory requirements.This is an ideal opportunity for a detail-oriented professional passionate about clinical research, compliance, and improving healthcare outcomes.The role provides exposure to complex global regulatory processes and opportunities to grow within a collaborative life sciences environment.