Deepthi Bidayat Email & Phone Number

Results-driven TMF Study Lead with a strong background in clinical research and expertise in document management. Proven track record of successfully leading and overseeing Trial Master File operations to ensure regulatory compliance, data integrity, and timely delivery of study documentation. Skilled in managing cross-functional teams, optimizing processes, and driving quality improvement initiatives. Committed to maintaining the highest standards of documentation excellence while adhering to industry best practices. Seeking to leverage my skills and experience to contribute to the success of clinical trials and make a positive impact in the pharmaceutical or biotechnology industry.Key Skills: - Trial Master File (TMF) Management - Regulatory Compliance & Quality Assurance - Document Control & Version Control - Cross-functional Team Leadership - Process Optimization & Efficiency - SOP Development & Training - Risk Management & Issue Resolution - Vendor Oversight & Relationship Management - Electronic Document Management Systems (EDMS) - Good Clinical Practice (GCP) Guidelines- Veeva Vault