Sr Process Associate
CurrentAs an eTMF Specialist, I manage and oversee the electronic documentation for clinical trials, ensuring compliance with regulatory requirements. My expertise lies in document management, where I ensure that all trial-related documents are accurately uploaded and maintained in the eTMF system. I conduct regular quality assurance audits to verify that all documents are complete and up-to-date.I collaborate closely with clinical trial teams, including project managers and clinical research associates, to facilitate smooth document flow and resolve any issues that arise. Additionally, I provide training and support to team members on best practices for using the eTMF system. With a strong focus on regulatory compliance, I stay updated on industry regulations to ensure our documentation meets all legal and ethical standards. I am passionate about contributing to the successful execution of clinical trials through effective document management.
