As a Clinical Research Coordinator, I am committed to accelerating clinical research and driving healthcare improvements by drawing on my technical skillset and expertise in supporting and overseeing end-to-end clinical activities with strict adherence to protocols and regulations.I streamline study operations by ensuring strategic alignment. To this end, I not only coordinate but also attend all key investor meetings to stay up-to-date with the latest and promote alignment with objectives and protocol updates while ensuring seamless meetings and discussions with the right documentation and resources in place.Secondly, I efficiently manage EDC systems ensuring data accuracy and completeness with on-time deliverables. For this, I strictly adhere to the timelines and cross-check all the data more than once by conducting internal audits to ensure external audit readiness. Additionally, I support CRA visits and external audits while also liaising with them on a regular basis.While managing the day-to-day activities of clinical trials, I secure compliance with regulatory requirements, institutional policies, ethical guidelines as well as study protocols. To this end, I leverage my intensive knowledge of the regulatory and policy protocols and changes while working closely with the investigator, CROs, sponsors, and other key stakeholders. Moreover, I always follow study protocols and maintain comprehensive documentation while aiding in the correct procedure implementation, which in turn enables me to further patient safety as well as study progress in spite of complicationsIf you’re looking for someone who drives clinical trials towards their success through efficient and on-protocol management of end-to-end clinical activities, I can be reached via email: ana.santos9529@gmail.com Key Skills: Study Timeline Management, Study Objectives Alignment, Study Sponsors and CRO Oversight, Quality Control, ICH-GCP Guidelines Adherence, Study Integrity, MyTrials, TOL, TrialMaster, Oracle Inform, iMedidata, OmniComm, Eurofins
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Ana S. Education Details
Frequently Asked Questions about Ana S.
What is Ana S.'s role at the current company?
Ana S.'s current role is Certified Clinical Research Coordinator ǀ Clinical Trials Management & Oversight | Clinical Trial Operations | Study Site & Timeline Management | Regulatory & Protocol Compliance | Quality Control | Study Data Management.
What schools did Ana S. attend?
Ana S. attended California State University, Los Angeles.
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