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Senior Statistical Programmer - 3 month contract

nh • Posted 5 days ago
Onsite Contract IT & Technology

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).

Skills and Experience Required

  • 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

Employment type

  • Full‑time

Job function

  • Science

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