Ana S.

Ana S. Email and Phone Number

Certified Clinical Research Coordinator ǀ Clinical Trials Management & Oversight | Clinical Trial Operations | Study Site & Timeline Management | Regulatory & Protocol Compliance | Quality Control | Study Data Management
Ana S.'s Location
Los Angeles, California, United States, United States
About Ana S.

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

Ana S.'s Current Company Details

Certified Clinical Research Coordinator ǀ Clinical Trials Management & Oversight | Clinical Trial Operations | Study Site & Timeline Management | Regulatory & Protocol Compliance | Quality Control | Study Data Management
Ana S. Work Experience Details
  • Nicr
    Lead Clinical Research Coordinator
    Nicr Mar 2024 - Oct 2024
  • Velocity Clinical Research, Inc.
    Clinical Research Coordinator Ll
    Velocity Clinical Research, Inc. Jul 2023 - Nov 2023
  • Dermatology Research Associates
    Certified Clinical Research Coordinator
    Dermatology Research Associates Aug 2021 - Jul 2023
  • Malibu Labs
    Cosmetic Chemist
    Malibu Labs Jan 2021 - Aug 2021
  • Gordon Labs
    Quality Control Chemist
    Gordon Labs Apr 2020 - Jan 2021
  • Esoterix
    Clinical Laboratory Techinician Il
    Esoterix Oct 2019 - Jan 2020
    Calabasas, California
  • Labcorp
    Laboratory Technician
    Labcorp Dec 2017 - Oct 2019
  • Ross Stores, Inc.
    Retail Associate
    Ross Stores, Inc. Feb 2016 - Oct 2018
    Greater Los Angeles Area

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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