Exciting Opportunity in Clinical Research - Join a Global Leader

Join the team as a global leader in the field of clinical research and make a significant impact in the biotech industry. We are seeking talented individuals for an exciting opportunity as part of a Full-Service Provider (FSP) team. As a member of this team, you will contribute to cutting-edge clinical trials and collaborate with industry experts to advance medical breakthroughs.

Company Background:

The organization is a renowned global leader in clinical research, providing comprehensive solutions to biotech companies worldwide. We pride ourselves on our dedication to excellence, innovation, and patient-centric approaches. As part of the Full-Service Provider (FSP) team, you will have the chance to work with a range of clients and contribute to meaningful projects.

Job Responsibilities:

• Develop and implement SDTM standards for clinical trial datasets in compliance with CDISC guidelines.
• Perform data manipulation, cleaning, and validation to ensure data quality and accuracy.
• Write and execute SAS programs to generate SDTM datasets, analysis datasets, and statistical outputs.
• Conduct statistical analyses and generate tables, listings, and figures for clinical trial reporting.
• Provide expertise and guidance on SDTM implementation and programming best practices to cross-functional teams.

Skills Required:

• Minimum 5 years of experience working with SDTM in clinical trials.
• Proficient in SAS programming and data manipulation.
• In-depth knowledge of CDISC standards, specifically SDTM.
• Strong understanding of clinical trial data management processes.
• Ability to perform statistical analysis and generate outputs.
• Attention to detail and commitment to regulatory compliance.

Location: South Africa

Employment Type: Permanent, Full-time

Salary: 900,000+ Rand

These roles will be filled quickly, apply below or directly to Max Trafford at Meet on Max.trafford@peoplewithchemistry.com. Feel free to call on 0044 203 019 6009, find out more about Meet at www.peoplewithchemistry.com

Associated Keywords: Senior Statistical Programmer, Clinical Trials, SDTM, SAS Programming, CDISC Standards, Data Analysis, Clinical Data Management, Statistical Analysis, Clinical Research, Biostatistics, Pharmaceutical Industry, Regulatory Compliance, Data Validation, Quality Control, Data Integration, Data Reporting, Data Manipulation, Statistical Modeling, Clinical Study Reports, Data Conversion, Clinical Database, Programming Languages, Statistical Software, Data Visualization.