Shashank Patil

About Shashank Patil

With two years of experience in Clinical Research, I bring a strong foundation in…

Experience

1. Clinical Process Co-ordinator

   IQVIA

   Jan 2024 — Present · Thane, IN

   I am responsible for ensuring smooth and timely site setup within the CTMS. My key responsibilities include:Responsible for the timely and accurate set-up of study sites within the Clinical Trial Management System (CTMS), supporting study start-up activities.Assisting in managing and maintaining the study site records in CTMS, including site correspondence essential emails.Preparing and maintaining study files, ensuring compliance with filing/naming guidelines in the electronic trial master file, and tracking document status.Resolving queries from cCRAs, Study Start-Up teams, and CRAs, providing prompt and accurate support regarding site builds and CTMS workflows.Ensuring smooth coordination between the study team and operations, maintaining continuity and alignment throughout the start-up phase.Consistently met internal service level agreements (SLAs) related to turnaround time, quality, and productivity for CTMS-related deliverables.Collaborate effectively with cross-functional stakeholders to support seamless execution of site activation activities and adherence to study timelines.Proactively address operational queries related to site creation and conducted 100% quality checks (QC) of assigned study sites within the CTMSOrganizing project team and client meetings, including scheduling, preparing meeting materials, binders, agendas, and minutes.

Education

• Sharadashram Vidyamandir Junior College of Science

  Higher Secondary Certificate

• Ramnarain Ruia College - Mumbai

  Pharma analytics sciences