Eligible Locations: India, UK, Ireland, Spain, Netherlands, Sweden, Poland, and South Africa.
Role Overview
This is a senior-level position within the clinical research and pharmaceutical domain. The role focuses on transforming raw clinical trial data into standardized formats and generating analysis-ready datasets for regulatory submissions (FDA, ICH, etc.).
Experience & Skills
Experience Level: 5+ years of strong professional experience.
Core Technical Competencies: * SDTM (Study Data Tabulation Model)
ADaM (Analysis Data Model)
TLF (Tables, Listings, and Figures)
Programming Languages: Likely requires high proficiency in SAS and/or R programming (based on hashtags).
Domain Knowledge: Clinical Data Analysis, CDISC standards, and regulatory compliance (FDA/ICH guidelines).
Key Responsibilities
Data Standardization: Mapping clinical data to CDISC standards (SDTM).
Analysis Programming: Developing ADaM datasets for statistical analysis.
Reporting: Creating TLFs to represent clinical trial results.
Regulatory Readiness: Ensuring datasets are “submission ready” with proper Define.XML and documentation.
Application Instructions
Primary Action: Reach out via email or LinkedIn Direct Message (DM).
To apply for this job email your details to adish.jindal@cytel.com
