Program and validate derived datasets, tables, figures, listings.
Process data from the external sources.
Perform ad hoc exploratory analyses for publications and programming support other functions of
Oversee programing work/deliverables from CROs.
Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification
Program and validate CDISC compliant deliveries for electronic submissions.

🎯 Requirements

Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related
BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the
Working knowledge of SAS and its various components.
Knowledge of R programming in clinical trials.
Familiarity with the drug development process.
Strong SAS and SAS Macro language skills.

🎁 Benefits

Training
Mentoring

🛃 Visa sponsorship

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