We are looking for Senior SAS Programmers who can also program in R with a background in working across clinical trials, ideally with experience in oncology.

The successful candidate will be proactive and conscientious in their work, with a customer focused mindset and a highly collaborative attitude, able to work closely with cross-functional teams to ensure effective data collection, manipulation, oversight and analytics-driven decision-making.

This is remote UK and you will need the right to work.

Key Responsibilities:

Data preparation: Prepare and organise data by identifying sources, defining structure, and performing mapping and integration activities to support analysis.

Anomaly detection: Identify anomalies within clinical trial data using advanced analytical techniques, be able to recognise the importance of those anomalies and explain those anomalies to a non-technical audience.

Quality Control: Conduct quality control activities to ensure the integrity of outputs and support the development journey of others through effective communication and analysis of quality control findings.

Requirements Analysis: Interpret requests and requirements from stakeholders into technical solutions that deliver high quality results.

Stakeholder communication: Collaborate with internal and external stakeholders to communicate data-driven findings and recommendations.

Regulatory Compliance: Ensure adherence to CDISC, Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements (FDA, EMA).

Skills and Experience Required:

This is an exciting opportunity for a data-driven professional to make a meaningful impact on clinical research and patient outcomes. If you have a passion for data analytics and clinical research, we encourage you to apply

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