RemotevilleRemote Principal Statistical Programmer Job in UK Worldwide Clinical Trials
Principal Statistical Programmer Worldwide Clinical Trials
£ -
CDISC StandardsComputer LiteracyMacrosNumeracyPossess Strong AnalyticalPro*CSASStatistical ProgrammingStudy Data Tabulation Model
Senior (5-8 years) - Expert (9+ years)
UK
As a leading full-service global CRO, we work to create solutions that advance new treatments from discovery to reality.
3355+ employees
B2BHealthcareScienceClinical Trials
Open for applications
Role
Who you are
- Possess expert level statistical programming skills across a variety of applications.
- Experienced in regulatory submissions and familiar with FDA and PMDA guidelines.
- Strong analytical skills and attention to detail are essential.
- Demonstrate excellent communication and leadership skills.
- Adept in training and mentoring new staff members.
Desirables
- Advanced SAS
- Mentorship Skills
- Process Improvement
- Regulatory Knowledge
What the job involves
- Lead and manage multiple complex studies as a project lead.
- Communicate effectively with both internal and external clients to manage expectations.
- Implement and oversee the application of advanced CDISC standards for data submission.
- Drive the development of process improvement projects and standard SAS Macros.
- Provide training and coaching to team members on Biostatistical Operations processes and tools.
Company
Company mission
Worldwide Clinical Trials is dedicated to advancing new treatments in partnership with biotechnology and pharmaceutical companies. With a focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, the organization utilizes a collaborative and personalized approach to develop solutions that improve patients' lives through innovative therapies.Company benefits
- Opportunity to lead in a global setting
- Team collaboration and support
- Professional growth and development
Company values
- Diversity
- Collaboration
- Innovation
- Quality