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Tier-1 employer, metro location, and mid-level experience increase applicant competition.
Clinical trial SDTM/ADaM and regulatory expertise limit transferability across industries.
Explicit 2-3 years plus mandatory SAS/R and SDTM/ADaM experience raises filtering strictness.
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Manage and deliver statistical programming tasks across clinical trials including SDTM/ADaM datasets, annotated CRFs, and TFLs in compliance with regulatory standards.
Contribute to trial setup activities such as eCRF development, metadata specifications, and clinical report support including CSRs and safety update reports.
Collaborate with internal/external stakeholders to ensure seamless trial execution and share best practices to optimize programming standards and processes.
Bachelor's or Master's degree in life sciences, natural sciences, engineering, or equivalent.
2-3 years programming experience with biological data or equivalent practical knowledge.
Proficiency in SAS or R programming languages and experience with clinical database technologies and data models.
Work Experience Required: 2-3 years of programming experience in relevant domain.
Experience operating within multinational and cross-functional clinical trial environments involving regulatory compliance.
Proven ability to manage variable workloads independently with accountability.
Strong analytical and communication skills enabling effective collaboration across regional and professional boundaries.