Senior Principal Statistical Programmer: Lead Trials

Novartis AG; City of Westminster; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical company in the United Kingdom is seeking a skilled Statistical Programmer to lead programming activities for clinical studies. The successful candidate will have expert experience in SAS and a strong understanding of regulatory requirements and industry standards. You will collaborate with cross-functional teams and ensure high-quality deliverables throughout the drug development process. If you are passionate about improving people's lives through innovative medicines, this role is for you.

Benefits

Personal and professional growth support

Diversity and inclusion commitment

Qualifications

• Minimum 3 years experience in a programming role, preferably in clinical trials.
• Advanced knowledge of industry standards including CDISC data structures.
• Experience as Trial/Lead/Project Programmer for multiple studies.

Responsibilities

• Lead statistical programming activities for multiple studies.
• Build effective relationships with cross-functional teams.
• Ensure compliance with company and industry standards in programming.

Skills

Expert SAS experience

Proven communication and negotiation skills

Ability to work with cross-functional teams

Understanding of regulatory requirements

Education

BA/BS/MS in statistics, computer science or related field

Tools

SAS

Job description

A leading pharmaceutical company in the United Kingdom is seeking a skilled Statistical Programmer to lead programming activities for clinical studies. The successful candidate will have expert experience in SAS and a strong understanding of regulatory requirements and industry standards. You will collaborate with cross-functional teams and ensure high-quality deliverables throughout the drug development process. If you are passionate about improving people's lives through innovative medicines, this role is for you.