ProPharma Group
Location
Hyderabad | India
Job description
Essential functions:
Provide statistical programming and validation for life sciences-related projects including clinical trial datasets and tables, listings, and figures.
Coordinate programming activities among the study programmers to achieve timely deliveries.
Access and convert data to SAS datasets and other file types from database management system and PC file formats (e.g., Microsoft Excel, text files).
Work with external vendors to develop and/or monitor the content and structure of SAS datasets and other files.
Oversee programming activities by external vendors (e.g., CROs).
Work closely with statisticians and other statistical programmers to generate and validate outputs to ensure accuracy and ensure the quality and soundness of statistical programming algorithms.
Provide input to specifications of tabulation and analysis datasets, validation plans, and other related documents.
Review data submission packages including define files, and data reviewers guide documents.
Mentor less-experienced statistical programmers.
Other duties as assigned.
Necessary skills and abilities:
In-depth knowledge of statistical programming.
Excellent communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.
Ability to program in SAS and/or R.
Educational requirements:
Bachelor's degree in Statistics, Computer Science, Mathematics, or a related discipline, or a combination of other education with 3+ years of relevant work experience.
Job tags
Salary
