Mayur Kotkar

Clinical SAS Programmer at STAR IT TECHNOLOGY
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Contact Information
us****@****om
(386) 825-5501
Location
Mumbai, Maharashtra, India, IN

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Credentials

  • SAS Certified Specialist: Base Programming Using SAS 9.4
    SAS
    Dec, 2022
    - Nov, 2024
  • Pharmacovigilance and clinical research
    Elite institute of pharma skills
    Oct, 2021
    - Nov, 2024
  • Pharmacovigilance Database training
    Clinevo Technologies
    Jul, 2021
    - Nov, 2024

Experience

    • India
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Clinical SAS Programmer
      • Jan 2023 - Present

      Collaborate with the client to understand requirements & forming clear requirement specifications. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Hands on experience on clinical trials dataset creation like Demographics (DM) Concomitant medication (CM), Adverse event (AE) & Medical history (MH), Vital Signs (VS) & Electrocardiogram results (EG). Developed SDTM Domains- DM, EX, AE, LB, TS, TI, TA, SU etc. Creating and… Show more Collaborate with the client to understand requirements & forming clear requirement specifications. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Hands on experience on clinical trials dataset creation like Demographics (DM) Concomitant medication (CM), Adverse event (AE) & Medical history (MH), Vital Signs (VS) & Electrocardiogram results (EG). Developed SDTM Domains- DM, EX, AE, LB, TS, TI, TA, SU etc. Creating and validating datasets, tables, listings, and figures (TLFs) for clinical study reports and regulatory submissions. Developed ADaM Domains. Conducting quality control checks on all SDTM Domains. Annotation of CRF as per Standards guidelines. Show less Collaborate with the client to understand requirements & forming clear requirement specifications. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Hands on experience on clinical trials dataset creation like Demographics (DM) Concomitant medication (CM), Adverse event (AE) & Medical history (MH), Vital Signs (VS) & Electrocardiogram results (EG). Developed SDTM Domains- DM, EX, AE, LB, TS, TI, TA, SU etc. Creating and… Show more Collaborate with the client to understand requirements & forming clear requirement specifications. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Hands on experience on clinical trials dataset creation like Demographics (DM) Concomitant medication (CM), Adverse event (AE) & Medical history (MH), Vital Signs (VS) & Electrocardiogram results (EG). Developed SDTM Domains- DM, EX, AE, LB, TS, TI, TA, SU etc. Creating and validating datasets, tables, listings, and figures (TLFs) for clinical study reports and regulatory submissions. Developed ADaM Domains. Conducting quality control checks on all SDTM Domains. Annotation of CRF as per Standards guidelines. Show less

    • United States
    • Software Development
    • 500 - 600 Employee
    • SAS Developer
      • Aug 2022 - Dec 2022

      Designed and developed new dashboard reports by importing and extracting data and then using data manipulation techniques t to achieve business requirements via SAS Enterprise Guide which will be used for reporting purpose with end-to-end visibility any issues that may happen in future. Refreshing and maintaining daily, weekly and monthly dashboard reports. Understanding and implementing changes in existing dashboard reports. Automating new as well as existing dashboard reports with… Show more Designed and developed new dashboard reports by importing and extracting data and then using data manipulation techniques t to achieve business requirements via SAS Enterprise Guide which will be used for reporting purpose with end-to-end visibility any issues that may happen in future. Refreshing and maintaining daily, weekly and monthly dashboard reports. Understanding and implementing changes in existing dashboard reports. Automating new as well as existing dashboard reports with the help of SAS macros to eliminate manual intervention. Converting existing Excel-base manual dashboard reports into SAS base automated dashboard reports. Show less Designed and developed new dashboard reports by importing and extracting data and then using data manipulation techniques t to achieve business requirements via SAS Enterprise Guide which will be used for reporting purpose with end-to-end visibility any issues that may happen in future. Refreshing and maintaining daily, weekly and monthly dashboard reports. Understanding and implementing changes in existing dashboard reports. Automating new as well as existing dashboard reports with… Show more Designed and developed new dashboard reports by importing and extracting data and then using data manipulation techniques t to achieve business requirements via SAS Enterprise Guide which will be used for reporting purpose with end-to-end visibility any issues that may happen in future. Refreshing and maintaining daily, weekly and monthly dashboard reports. Understanding and implementing changes in existing dashboard reports. Automating new as well as existing dashboard reports with the help of SAS macros to eliminate manual intervention. Converting existing Excel-base manual dashboard reports into SAS base automated dashboard reports. Show less

    • India
    • IT Services and IT Consulting
    • 1 - 100 Employee
    • Trainee Clinical Data Analyst (SAS Programmer )
      • Jul 2021 - Jul 2022

      Completed training on SAS Programming. Implementing and maintaining standard programming practices and processes to ensure consistency and efficiency in programming activities. Developing and maintaining SAS programs for the analysis and reporting of clinical trial data. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Annotation of CRF as per Standards guidelines. Completed training on SAS Programming. Implementing and maintaining standard programming practices and processes to ensure consistency and efficiency in programming activities. Developing and maintaining SAS programs for the analysis and reporting of clinical trial data. Preparing STDM and Validating SAS programs as per client assignment specifications according to SDTM Standards. Annotation of CRF as per Standards guidelines.

Education

  • MGV's pharamcy college
    Bachelor of Pharmacy - BPharm, Pharmacy, Pharmaceutical Sciences, and Administration
    2017 - 2021
  • Savitribai Phule Pune University
    Bachelor of Pharmacy - BPharm, Pharmaceutical Sciences
    2017 - 2021

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