Senior Statistical Programmer (Contract)
Warman O'BrienSevilla, Andalucía, EspañaHace 3 días
Descripción del trabajoBachelor’s degree in Computer Science, Statistics, or a related field with 5+ years of clinical programming (CDISC) experience, or Master’s degree with 6+ years of experience. Proven experience in Oncology therapeutic area. Strong understanding of ICH / GCP guidelines, clinical trial processes, and regulatory standards. Solid knowledge of the drug development lifecycle and submission processes. Excellent communication, coordination, and stakeholder management skills. Demonstrated ability to manage multiple priorities and meet deadlines efficiently. 6-12 month contract (possible extension) Competitive hourly rate Remote Start Date : ASAP
We are seeking an experienced Senior Statistical Programmer Consultant to support one of our key clients in the pharmaceutical industry. This is a FSP position suited to a confident professional who can work independently while fostering strong, trust-based relationships with sponsor counterparts.
Key Responsibilities
- Lead and support programming deliverables for clinical studies and projects.
- Implement statistical programming aspects of study protocols and clinical development plans.
- Deliver high-quality, efficient programming outputs and ensure compliance with standards and automation tools.
- Prepare and review specifications, ensuring documentation is complete and accurate.
- Contribute to process improvement and best practice development within the programming function.
- Collaborate closely with cross-functional teams including Biostatistics, Data Management, and Project Leadership.
- Proactively identify and elevate project risks where necessary.
Requirements
Details
If you would like to know more, apply here or get in touch.
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Senior Statistical Programmer • Sevilla, Andalucía, España
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