MERCK GROUP Hiring Clinical SAS & R Programmers (Associate Principal Statistical Programmers)
MERCK GROUP Hiring Clinical SAS & R Programmers (Associate Principal Statistical Programmers)
Job Description:
Your Responsibilities include, but are not limited to ADAM Datasets development
- Table / Listing / Figure (TLF) development and validation based on the Statistical Analysis Plan
- TLF Mock shells development
- Perform programming activities on asset level in Integrated ADAM Datasets development incl. creation of specifications
- TLF Mock shells development for integrated analysis like ISS or ISE
- Table / Listing / Figure (TLF) development and validation based on the Statistical Analysis Plan
- Performing ad-hoc programming activities based on internal and external requests
- Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning
- Collaborates effectively within statistical programming and cross-functional project team and with counterparts to achieve the project goal
Qualifications: BSc or MSc in Computer Science, Mathematics, Statistics, or related health science 6+ years of experience in the pharmaceutical industry including support of regulatory filings. Experience in an international environment is a plus. R and SAS practical and effective knowledge good knowledge of CDISC standards (SDTM and ADaM including specifications)Good knowledge of drug development process, industry standards, and statistical concepts
work Location: Electronic City Phase 1, Bangalore
APPLICATION PROCESS; Interested Candidates can share their resumes with [email protected]
A Clinical SAS Programmer is a person who specializes in using SAS (Statistical Analysis System) software to analyze and manage data for clinical trials. This person would be responsible for writing and maintaining SAS programs to extract, manipulate, and analyze data from clinical studies. They would also be responsible for creating tables, listings, and figures for study reports and regulatory submissions.
The Clinical SAS Programmer would work closely with the clinical trial team, including statisticians, data managers, and other programmers, to ensure that the data is accurate and meets the requirements of the study. They would also be responsible for ensuring that the data is in compliance with regulatory guidelines and standards. Additionally, they may also be responsible for creating and validating datasets for submission to regulatory agencies.
The role of a Clinical SAS Programmer can be critical for the success of clinical trials, as they are responsible for providing the data that forms the basis of the trial’s conclusions, and regulators rely heavily on the data in determining whether to approve drugs or medical devices.
