Ubed S.

About Ubed S.

Being at Zelta as a Senior Study Delivery Lead offering EDC platform solutions for clinical trials in various therapeutic areas like Oncology, Immunology, Dermatology, Vaccines, Endocrinology, and so on.We provide one point solution with various EDC package modules like Drug Dispense, Randomization, ePRO/eCOA, Medical Coding, Training Tracking, Local Labs with reduced study build time.Clinical Data Manager with the significant amount of experience in the field of CDM in various clinical studies and in all clinical phases, performed extensive amount of data management skills in various EDC databases including Medidata, Rave, and Oracle-clinical and phase forward Inform, and has developed excellent knowledge of industry wide standards and best practice. Has complete exposure to clinical data management of multiple studies with all clinical phases in multiple projects with key emphasis on developing and maintaining data management plan (DMP), data transfer agreements and worked during study start-up on CRF designing, and created edit checks, query logics and user acceptance testing (UAT) on various platforms.Clinical support in all phases during study conduct on validating the data, cleaning the data, discrepancy management, lab reconciliation, SAE reconciliation and worked extensively on study initiation, study conduct, and study closeout and database lock activities.

Experience

1. Senior Study Delivery Lead

   Merative

   May 2023 — Present · Hyderabad, IN

   Collaborate with global Training & Services lead to shape service offerings, identify gaps and opportunities to expand and grow the team.· Collaborate to build talent/capabilities within the team to support offerings & growth.· Delight customers through on-time, first time right, quality delivery of contracted scope of services. · Enable the success of the team through training, mentoring using different leadership methods.· Lead and work alongside the team to ensure objectives and deliverables are met.· Track team progress, objectives, and projects· Effectively develop/encourage collaboration within the team to meet key performance indicators.· Prioritize issues assigned and ensure those issues are completed within a given timeline and with minimal supervision· Manage the workload, schedule, and productivity of the team· Pursue a program of self-development with selected reading, seminars, and participation in continuing education and represent Merative in industry forums · Identify and communicate possible improvements in the work process for customers, product, and peers· Perform other duties as assigned by immediate supervisor or upper management.

Education

• ICRI

  MSc Clinical Research, Clinical Research

  2009 — 2011

• Yeshwant college of Bioinformatics & Biotechnology

  Bioinformatics, Bioinformatics

  2006 — 2009

• Cranfield University

  Master of Science (MS), Clinical Research

  2009 — 2011