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Job Description
Structured overview of role & requirementsAbout This Role
Lead design, development, and validation of complex clinical data programming using SAS, Python, R, SQL, and dashboard tools to support global clinical trials.
Build and maintain dashboards and reports to improve trial oversight, data cleaning, and operational performance, enabling faster evidence-based decision-making.
Drive project initiatives aligned to clinical programming roadmap, set programming standards, manage quality and risks, and mentor junior programmers.
Minimum Requirements
Bachelor’s or Master’s degree in computer science, life science, or statistics or equivalent.
Strong programming skills in SAS, Python, R, SQL, and dashboard technologies like Power BI or Spotfire.
Proficient knowledge of clinical development process and industry standards including experience with EDC systems (e.g., Medidata Rave, Veeva) and data platforms (e.g., Saama, SAS LSAF).
Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Experienced in programming and reporting within clinical trials focused on multiple therapeutic areas including cardiovascular, renal, metabolic, respiratory, and immunology.
Capable of independently leading programming initiatives that scale across studies and functions and influencing cross-functional teams.
Skilled in combining technical programming expertise with knowledge of clinical processes to improve data quality, efficiency, and compliance.