> Supported client in streamlining the redaction process as an integrated role with the sponsor> Handling review and approval of documents> Study team communication and leading client calls> Quality reviews of redacted documents> Knowledge transfer to new joiners

> Clinical trial disclosure: Registration of clinical trial protocol and results of clinical and non-clinical studies on different public registries along with the maintainance of protocol amendments> Redaction and Anonymization: Involved in various redactions compliant with EMA policies 0073, 0043, HC PRCI, etc. Managed bulk documents transitioning from EudraCT to EU CTIS.> Regulatory Intelligence: Maintained a comprehensive understanding of global regulatory frameworks governing clinical trial transparency, ensuring ongoing compliance.> Drafted informative regulatory sections for inclusion in monthly newsletters, facilitating sponsors awareness and engagement.