Suraj Chaurasiya
Clinical Process Coordinator 2 @IQVIA
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WORK HISTORY
Clinical Process Coordinator 2 @IQVIA
Thane, IN
Role Overview:Preparing and monitoring reports, perform standard monitoring activities for studies, managing queries (Communications), managing samples and kit shipment, loading and updating sites in LTMS databases, providing portal access to the sites, co-ordinate with Lab, CTM, clinical team and project services.1. On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc.) and related assessment.2. Under minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to:a) Loading and updating the active databases with details of participating sites.b) Provisioning of access for LTMS Portal.c) Monitoring on-time release of patient laboratory report by query management.d) Ensuring that documentation is available for all monitoring activities performed for real-time audit readiness.3. To monitor the day to day running of designated projects, including patient specimen management receipt, pending test lab report to PM team, and other duties as detailed in the project specific monitoring plan. Liaising with other internal departments (Lab, Lab Ops and Specimen Management) in order for all appropriate process occurring according to schedule.4. Data Reconciliation, Initial Kit Shipment, Courier Set up (CBCO and LCT/LPT).
EDUCATION
K V Pendharkar College of Arts Science and Commerce
HSC , Science
Guru Nanak Khalsa College of Arts Science & Commerce
Bachelor of Science, Bioanalytical Sciences
Saraswati Vidhya Mandir
SSC, General
ABOUT SURAJ CHAURASIYA
Goal-oriented professional with 3.5 + years of experience as a Clinical Process Coordinator describing my expertise in handling Study right from startup phase, followed by study conduct till study closeout by providing support on CTMS platform. Performing administrative task on assigned trials including Clinical data monitoring, query management, delivering periodic reports and knowledge of the drug development process with a considerable understanding of ICH-GCP. Highly skilled in reasoning and problem solving and can work as an individual and as a part of a team. Outstanding ability to plan, analyze and accomplish the Clinical Data Base Management objective in a timely manner.
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