Pandiarajan P

Experience

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  Cognizant

  May 2007 - May 2010

  Responsibilities: Perform the technical review of eCRFs and review the Data Validation Specification. Develop SQLs to handle ad-hoc requests. Handle custom activities including Lab Upload, Data Load. Create Data Mappings for Trial Data Extracts (TDE).Honors and Awards: Got perfect score in every appraisal completed. Received many appreciations from sponsors. Got the ‘Associate of the Quarter’ award once. Received the ‘Associate of the month’ award twice. Show less

  • Programmer Analyst

    May 2008 - May 2010

  • Programmer Analyst Trainee

    May 2007 - Apr 2008
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  ICON Clinical Research India Private Limited

  May 2010 - Dec 2012

  Responsibilities: Act as a Team Lead for 5-8 members team. Support Manager in performing interim/annual performance appraisal of assigned team members and identifies gaps and proposes development plans.  Ensure effective resource allocation and workload balancing across assigned team members.  Extend technical expertise and mentor team members on an ongoing basis.  Ensure team achieves productivity and quality targets, perform benchmarking reviews and perform oversight of deliverables using different tools/techniques and maintain and report relevant metrics. Show less

  • Team Leader

    Nov 2012 - Dec 2012

  • DBA II

    Apr 2011 - Oct 2012

  • DBA I

    May 2010 - Mar 2011
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  Clinical Data Programming Lead I

  Jan 2013 - Mar 2015

  Clinical Data Programming Lead I

  Responsibilities: Act as a Project Lead for the assigned studies. Coordinate between programmers and testers to ensure the quality of deliverables. Attend sponsor meetings to discuss about requirements and show demo to them. Organize meetings between programmers and study team as required to understand the requirements and deliver the projects as per the requirements. Working with multiple projects at the same time and manage maintenance tasks of the studies as well. Participate in internal audits and take ownership of the findings.Honors and Awards: Got perfect score in every appraisal completed. Received multiple appreciations from internal/external customers. Show less

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  ICON Clinical Research India Private Limited

  Apr 2015 - Mar 2016

  Responsibilities: Responsible for leading and overseeing set-up and maintenance as well as providing advanced technical support related to Clinical Data Management Systems required for clinical studies. Review requirement documents created by study team and share expert advice whenever needed. Trouble-shoot and solve study build issues and edit check programming issues. Perform an Impact Analysis and Risk Assessment of the proposed changes.Honors and Awards: Got ‘Standing Ovation’ award (one of the prestigious award) for the exceptional project delivery throughout the year 2015. Got ‘Cheer’ award for the work done on ‘Lilly Procedure re-design’. Got perfect score (5 out of 5) in appraisal. Show less

  • Clinical Data Programming Lead

    Jun 2015 - Mar 2016

  • Clinical Data Programming Lead II

    Apr 2015 - Jun 2015
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  ICON Clinical Research

  Apr 2016 - Sept 2019

  Senior Clinical Data Programming Lead

  Responsibilities: Acting as a backup for Manager. Overseeing deliverables for different clients, specifically to the full service provider (FSP) portfolio. Working with colleagues to act as a maven for client specific deliverables.  Act as a Subject Matter Expert for global studies. Act as an ICON representative to support different portfolios and vendors.  Working directly with sponsor to identify gaps in their process, suggest process improvements, prepare process related documents and roll out the same to other TPOs. Sharing innovative thoughts to streamline sponsor process and closely work with them to implement the same. Suggest process improvement thoughts within the organization and prepare required process documents for the same. Working for global studies and share expert advice for the effective design of the Electronic Data Capture (EDC) Case Report Form(CRFs). Taking administrative responsibilities include forecasting the planning and tracking of projects, resource allocation, and supervision of programmers and testers. Providing training to the programmers, testers, peers, and study teams to support the process and improve the quality. Providing training on the new technologies rolled out to the programmers and peers. Participate in both internal/external audits and act as a point of contact from programming to quality control of documentation. Effectively coordinating with study team during study build development/maintenance phase and support them as required.Honors and Awards: Received appreciation from sponsor for the tool developed. Got ‘Take a Bow’ award for the project delivered. Received appreciation from sponsor for the contribution towards their process improvements. Show less

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  ICON plc

  Oct 2019 - now

  • Senior Manager

    Apr 2024 - now

  • Manager Data Management

    Oct 2019 - Apr 2024