Senior Statistical Programmer (Contract)

Warman O'Brien; Pamplona; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading consultancy in the pharmaceutical sector is seeking a Senior Statistical Programmer Consultant in Pamplona, Spain. This 6-12 month remote contract requires a professional adept in clinical programming, particularly in oncology. The ideal candidate will have a strong grasp of ICH/GCP guidelines and excellent communication skills. This role offers competitive hourly rates and the potential for contract extension.

Formación

• 5+ years of clinical programming experience (CDISC).
• Strong understanding of ICH / GCP guidelines.
• Ability to manage multiple priorities efficiently.

Responsabilidades

• Lead and support programming deliverables for clinical studies.
• Implement statistical programming aspects of study protocols.
• Prepare and review specifications ensuring documentation accuracy.

Conocimientos

Clinical programming

Oncology expertise

Communication skills

Stakeholder management

Educación

Bachelor’s degree in Computer Science, Statistics, or a related field

Master’s degree in relevant field

Descripción del empleo

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

• Bachelor’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.

Details

• 6-12 month contract (possible extension)
• Competitive hourly rate
• Remote
• Start Date: ASAP

If you would like to know more, apply here or get in touch.