Diganta Bose
Senior Statistical Programmer at Cytel- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
-
English Full professional proficiency
-
Hindi Native or bilingual proficiency
-
Bengali Native or bilingual proficiency
Topline Score
Bio
Credentials
-
SAS Certification in Base SAS
SAS
Experience
-
Cytel
-
United States
-
Pharmaceutical Manufacturing
-
700 & Above Employee
-
Senior Statistical Programmer
-
Mar 2020 - Present
-
-
Senior Team Lead - Statistical Programming
-
Aug 2013 - Mar 2020
My day to day activities requires working closely with Biostatistician(s) , understand the statistical analysis and reporting of the data and eventually implement and deliver outputs by writing SAS programs. These programs re-arrange or reform the data (tabulation) , analyse it, and finally present reports in the form of tables, listings and graphs(or figures). Interaction with Clinical Data management team may also be required at times in order to identify discrepancies and get them corrected. Not only writing programs for generating Statistical Outputs, but also at times Validation and Quality Control of Statistical Outputs generated by others is a frequent activity. I have been supervising similar technical activities in my team and handle projects independently. The project related activities include programming and writing specifications for CDISC (SDTM and ADAM) and non CDISC datasets, reports Like TLFs and specific adhocs and so on. Basically each project involves end to end Statistical programming activities.I also, like many statistical (SAS) programmers, have keen interest in developing useful and robust SAS utility programs that help in increasing productivity. I keep developing such SAS macros whenever I get some free time.
-
-
-
Cognizant
-
United States
-
IT Services and IT Consulting
-
700 & Above Employee
-
Analyst-SAS Programmer
-
Aug 2012 - Aug 2013
Programming and Validation for SDTM and Analysis Datasets, Tables, Listings and Graphs. Creating Programming Specifications for SDTM MappingProgramming for Patient Listings and other non-submission internal reportsCRF Annotations as per SDTM Guidelines Programming and Validation for SDTM and Analysis Datasets, Tables, Listings and Graphs. Creating Programming Specifications for SDTM MappingProgramming for Patient Listings and other non-submission internal reportsCRF Annotations as per SDTM Guidelines
-
-
-
MMS
-
United States
-
Pharmaceutical Manufacturing
-
400 - 500 Employee
-
Clinical SAS Programmer
-
Apr 2010 - Aug 2012
I work for MMSH Clinical Research Private Limited which is the Asia Operations for Parent Company MMS Holdings Inc. based in Canton,Michigan,USA.I work as a SAS Programmer, writing programs for analysis of Clinical Data, generating CDISC Complaint Data Structures(SDTM and ADaM), generating Tables and Listings, generating Patient Profiles or Patient listings and double programming validation of outputs.I am a certified programmer for Base SAS 9 and currently looking forward to write advanced SAS certification very shortly.Apart from SAS programming I also worked with Clinical Data Management team to Annotate CRFs. I am also trained in Quality Control of ISS and ISE Tables.
-
-
-
-
Graduate Assistant
-
Aug 2007 - Dec 2008
Worked in Bioinformatics research projects and also took part in teaching Biological Principles to Undergraduate Students. Worked in Bioinformatics research projects and also took part in teaching Biological Principles to Undergraduate Students.
-
-
Education
-
Georgia Institute of Technology
Master of Science (MS), Bioinformatics -
Bapuji Institute of Engineering and Technology
Bachelor of Engineering, Biotechnology