Principal Programmer

• Oct 2019 - Present

Statistical Programmer II

• Sep 2018 - Sep 2019

 Lead programmer providing subject-matter expertise for the design, planning, strategy proposal and decision-making of programming tasks at study and project levels. Key person accountable for heading programming activities as Trial Programmer for several studies of medium to the large sized project in phase I to IV clinical studies. Responsible for performing, planning and monitoring the development, implementation andvalidation of new process technologies, macros and applications, intricately understanding risk factors and alerting team on potential milestone slippages. Ensuring timely and quality development and validation of datasets and outputs for CSRs, regulatory submissions, safety reports, publications, post-marketing activities or exploratory analyses (as required) in the assigned studies. Further responsibility to provide deft training sessions to statistical programming teams and recruits;also undertaking standardization of reporting procedures for graphical and tabular reports.

Assistant Manager

• Jul 2017 - Sep 2018

 Lead Programmer supervising a team of 6 to allocate work and co-ordinate on-time and seamless delivery of project outcomes with successful study lock. Key ‘Point-of-Contact’ for all client communications, dealing with issues, resolving regular queries and negotiating deadlines for smooth study deliveries. Responsible for furthering as an independent programmer, testing for programming and developing and validating SAS macros for programs. In-charge of the maintenance of software applications, identifying enhancements, recommending on new features and performing requirement and SAS program review. Ensured traceability and regulatory compliance by maintaining all supporting documents for studies in accordance with WSOPs/Guidelines. Part of my job was to develop, train and mentor the team on both functional and professional aspects to include KSAs about processes, standards and SAS for fresh associates.

Business Process Lead

• Sep 2014 - Jul 2017

Staistical Programmer II

• Jan 2013 - Sep 2014

 Worked as a key statistical programming and quality control support for the phase II-III studies,collaborating with external and internal cross-functional teams to provide advanced technicalexpertise across complex studies with an aim to fulfil multiple project deliveries. Generated draft and final sets of summary data tables and analyses as part of clinical study reportsand ISS/ISE documents for regulatory submission. Developed and validated SAS macros, templates, datasets, tables, listings and figures, along withutilities for data cleaning and reporting. Developed programming standards and checked for both consistency and adequacy to ensure CRFmeets protocol guidelines. Compiled extensive reports and communicated project status to the senior management andappropriate working teams.

Statistical Programmer I at Lilly Venture (i3)

• Sep 2011 - Dec 2012

 Responsible for designing and planning the overall approach to a project’s programming tasks, working across development, implementation and validation of new process technologies, macros andapplications. Undertook programming, testing and documentation of statistical programs for use increating statistical tables, figures and listings. Used SAS data step programming, various procedures, additional methodologies and advancedprogramming such as macros, ODS, SQL, SAS STAT and SAS Graph, effectively. Performed quality control checks for source data and reported data issues periodically.

ITP

• Jun 2008 - Apr 2009

Worked SCPs and video analytic's and designed a de-interlacer with motion detection and motion compensation