Senior Clinical Research Associate
Current• Achieved high adherence to the approved monitoring plan, collaborating with project team members to resolve most of the issues encountered, ensuring smooth participation in the investigator payment process.• Provided regular updates to the Clinical Team Manager (CTM) and study team members, highlighting important trends across multiple sites, resulting in the implementation of targeted strategies that improved site performance.• Configure Veeva applications using Veeva custom settings, Veeva messages, and section signals on page layouts, offline validation rules, sample management Functional.• Delivered effective presentations and reports, resulting in a good understanding and appreciation of task accomplishments among stakeholders, positively impacting project engagement and buy-in.• Involved in implementing various modules of Veeva - Closed Loop Marketing (CLM) Browse, Engage, Veeva Vault and Approved Email functionality.• Ensured completeness and compliance of essential documents as per ICH-GCP and applicable regulations, conducting thorough on-site file reviews that resulted in few findings during audits.• Documenting and streamlining Veeva Vault intake workflows with BPMN, Scrum, workflow optimization methods. Documentation of Veeva Vault Intake processes for sales aids, approved e-mail.• Generated comprehensive trial status tracking reports and progress updates for the CTM, leading to informed decision-making and proactive adjustments that reduced study delays.• Facilitated effective communication among investigative sites, the client company, and the project team, resulting in a reduction in communication errors and improved collaboration.• Maintained a high accuracy rate and timely completion of administrative tasks, including expense reports and timesheets, ensuring efficient financial tracking and saving time for the project team.
