Match Score
Against your primary resumeLogin to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 CRO, Bangalore metro role with niche SAS/CDISC skills, moderate applicant density.
Clinical trial CDISC/SAS expertise is highly domain-specific and not easily transferable across industries.
Mandatory SAS, CDISC/ADaM/SDTM expertise and regulated clinical trial experience enforce strict technical filtering.
Job Description
Structured overview of role & requirementsAbout This Role
Lead statistical programming activities across multiple clinical trial data projects, ensuring data integrity and adherence to regulatory standards.
Develop, validate, and review datasets and outputs using SAS programming with compliance to CDISC standards (ADaM, SDTM).
Mentor junior programmers and collaborate cross-functionally to align programming deliverables with project timelines and regulatory requirements.
Minimum Requirements
Bachelor's degree in Statistics, Computer Science, or related field; Master's degree preferred.
Proficiency in SAS programming and statistical software tools relevant to clinical trials.
Experience in a regulated environment with strong knowledge of regulatory requirements for clinical trial data.
Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Experienced leader capable of managing and mentoring teams while driving process improvements in statistical programming.
Skilled in delivering complex programming solutions under tight deadlines within clinical research settings.
Strong collaborator adept at liaising between data management, biostatistics, and other departments to ensure high-quality outputs.