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:

• Lead and oversee the implementation of SDTM standards for clinical trial datasets, ensuring adherence to CDISC guidelines.
• Develop and validate complex SAS programs to generate SDTM datasets, analysis datasets, and statistical outputs.
• Provide technical expertise and guidance to cross-functional teams on SDTM programming and best practices.
• Collaborate with stakeholders to define and execute statistical analysis plans and contribute to clinical study reports.
• Ensure quality and integrity of clinical trial data through comprehensive review, validation, and documentation processes.

Skills Required:

• Minimum 8 years of experience in statistical programming, specifically with SDTM standards and CDISC guidelines.
• Expertise in SAS programming, data manipulation, and statistical analysis in a clinical trial setting.
• In-depth knowledge of SDTM implementation, controlled terminology, and data mapping principles.
• Strong understanding of regulatory requirements and industry best practices in clinical research.
• Excellent problem-solving skills, attention to detail, and ability to effectively communicate complex concepts to diverse stakeholders.

Location: South Africa

Employment Type: Permanent, Full-time

Salary: 1,150,000+ 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.