Senior Statistical Programmer
Listed on 2026-02-12
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Business
Data Scientist, Data Analyst
Senior Statistical Programmer – 3 month contract
Join to apply for the Senior Statistical Programmer – 3 month contract role at Coronado Research
.
We are looking for a Senior Statistical Programmer to support a key customer for a period of 3 months. 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.
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, recognise the importance of those anomalies and explain them 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).
- Extensive experience creating and validating SDTM and ADaM datasets to CDISC standards.
- Generation and QC of complex Tables, Listing and Figure (TLF) outputs.
- Bachelor’s or higher degree in a scientific, technical, or data‑driven discipline.
- Proven experience of working with clinical data.
- Extensive experience with SAS for data manipulation and analysis. Other programming languages such as R or Python would be beneficial.
- Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and global clinical trial regulations.
- Ability to diagnose data discrepancies, apply critical thinking, and generate actionable insights.
- Excellent logical, analytical and problem‑solving skills.
- A conscientious approach to accuracy to ensure data reliability and compliance.
- Good customer focus, able to prioritise the needs and satisfaction of our customers and address and resolve conflicts constructively, respectfully and with resilience.
- Ability to work both independently and collaboratively in a fast‑paced, cross‑functional environment.
- Dependable and a commitment to maintaining high data quality standards through a conscientious approach.
- Strong communication and interpersonal skills for effective collaboration across teams.
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.
#SAS #statisticalprogramming
Seniority level- Mid‑Senior level
- Full‑time
- Science
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