Senior Statistical Programmer

Senior/Principal Statistical Programmer | Small CRO | Remote/Hybrid We're partnered with a small CRO who are experiencing a large amount of growth within Biometrics. The Role: As a Senior Statistical Programmer, you'll lead high-impact projects, tackling complex statistical programming tasks and managing project timelines. You'll work directly with clients and regulatory agencies, ensuring data quality and delivering programming solutions for clinical trials. You’ll also have the chance to mentor junior team members, contribute to regulatory submissions, and develop new programming tools. Key Responsibilities: Lead statistical programming for complex projects, solving intricate challenges while ensuring project delivery meets quality standards. Collaborate with clients, providing programming oversight, project estimates, and participating in bid defenses. Contribute to regulatory submissions and represent the company in regulatory discussions. Create and validate SDTM and ADaM dataset specifications, ensuring adherence to SOPs. Program and validate datasets, ensuring accuracy and data integrity. Mentor junior programmers and lead project teams, fostering development and collaboration. Innovate by developing macros, utilities, and tools to enhance efficiency. Implement data integrity checks, ensuring scientific accuracy and quality. Qualifications: Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science. 6+ years of clinical trial statistical programming experience with a Masters Degree or higher in a Statistical related subject. Experience working with clinical trial data, SDTM/ADaM datasets, and regulatory submissions. What to do next? Apply now to avoid missing out on this opportunity!

As a Senior Statistical Programmer, you will lead high-impact projects and manage complex statistical programming tasks. You will collaborate with clients and regulatory agencies to ensure data quality and deliver programming solutions for clinical trials.

Candidates should have a Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science, along with 6+ years of clinical trial statistical programming experience. Experience with clinical trial data, SDTM/ADaM datasets, and regulatory submissions is also required.

• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Statistical Programming
• Clinical Trials
• SDTM
• ADaM
• Data Quality
• Regulatory Submissions
• Mentoring
• Project Management
• Data Integrity
• Programming Solutions
• Biometrics
• Macros
• Utilities
• Epidemiology
• Biostatistics
• Computer Science

• Science & Research
• Healthcare
• Data & Analytics
• Technology
• Consulting

Formation minimale

Maîtrise

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Mid-Senior level

Mode de candidature

La candidature directe est offerte