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 competitivenessStrong Tier‑1 brand and metro location but specialized clinical/CDISC skillset limits applicant density.
Clinical trial, CDISC, and regulatory-specific skills make cross-industry transitions difficult.
Explicit 8+ years, mandatory SAS/CDISC expertise and vaccines experience create strict shortlisting filters.
Job Description
Structured overview of role & requirementsAbout This Role
Lead planning and execution of statistical programming deliverables for vaccine projects across pre-clinical to clinical stages, ensuring quality and timeliness.
Oversee creation and review of study documents, specifications, and compliant CDISC data packages in line with Health Authority expectations.
Guide junior staff, perform quality control, and manage integrated analyses across multiple studies for reporting and regulatory submissions.
Minimum Requirements
8+ years of experience in statistical programming within clinical research, including some vaccines experience.
Proficient in SAS programming (BASE, STAT, MACRO, GRAPH, SQL) and familiar with R; experienced in CDISC SDTM/ADaM standards specific to vaccines.
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related health sciences.
Work Experience Required: 8+ years statistical programming experience; Notice Period: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Experienced leader with a record of successfully managing multiple concurrent vaccine-related clinical studies/projects.
Strong expertise in complex programming solutions, quality control, and project management within biostatistics/statistical programming teams.
Capable of independently drafting specifications and handling integrated data analyses for regulatory and publication purposes.