Senior Clinical Data Analyst

4 weeks ago


Anywhere in IndiaMultiple Locations ApicalGo Consultancy Full time
Job Title: Senior SAS Programmer/Lead Programmer

Job Summary:

The Senior SAS Programmer/Lead Programmer is responsible for designing, developing, evaluating, and modifying computer programs to analyze and evaluate clinical data. This role requires a strong understanding of programming languages, databases, and regulatory standards.

Key Responsibilities:

  • Collaborate with statisticians and other functions to plan clinical programming deliverables, including data cleaning, extraction, and integration programs.
  • Develop and review programming specifications for various types of deliverables, applying SAS programming.
  • Contribute to the development of Data Management and Validation Plan, Statistical Analysis Plan, and other related documents.
  • Perform all other project and process-related activities assigned by the supervisor, such as documentation of deliverables, timelines, and client communication.
  • Contribute to on-going data quality improvement efforts within assigned projects using SAS and other proprietary software.
  • Maintain quality and timeliness of assigned project activities and perform control checks with help of other team members for all the generated reports.
  • Work with the programming teams and projects to ensure timeliness and quality of deliverables.
  • Significantly contribute in implementing process improvement programs.
  • Provide data on productivity, quality, and timelines regularly to supervisor.

Requirements:

  • Master's Degree/Bachelor's Degree in Mathematics, Statistics, Engineering, Computer Science/Applications, Pharmacy, or any other similar type of qualification.
  • At least six years (Lead)/Four years (Senior) of Clinical SAS programmer experience in Pharmaceutical/CRO.
  • Good knowledge of programming languages (SAS Macros, SQL, STATS, graph, and ODS) with an understanding of databases.
  • Knowledge of CDISC SDTM and ADaM models and data mapping process is desirable.
  • Good analytical skills with the ability to process scientific and medical data.
  • Knowledge of regulatory submission process.
  • Knowledge in development, documentation, and testing of analysis data and programming code to meet regulatory and company standards.
  • Understanding of GCP principles and other regulatory standards in Clinical Research.
  • Good organizational and communication (written and oral) skills, ability to manage multiple tasks, ability to work with minimum supervision, as well as in a team environment and a desire to improve skills.

About Us:

ApicalGo Consultancy is a leading provider of clinical research services, dedicated to delivering high-quality solutions to the pharmaceutical and biotechnology industries.



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