Senior Statistical Programmer

Warman O'Brien; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

A leading company in the Biometrics sector is seeking a Senior Statistical Programmer to lead high-impact projects and manage statistical programming tasks. This role involves direct collaboration with clients and regulatory agencies, mentoring junior team members, and developing programming tools. The ideal candidate will have a strong background in clinical trial data and statistical programming, ensuring data quality and integrity.

Qualifications

• At least 6 years of clinical trial statistical programming experience with a Master’s degree or higher.
• Experience with clinical trial data, SDTM/ADaM datasets, and regulatory submissions.

Responsibilities

• Lead statistical programming for complex projects, ensuring quality and timely delivery.
• Mentor junior programmers and lead project teams to foster development and collaboration.
• Develop macros, utilities, and tools to improve efficiency.

Skills

Statistical Programming

Data Integrity

Mentoring

Education

Master’s or Ph.D. in Statistics

Master’s or Ph.D. in Biostatistics

Master’s or Ph.D. in Epidemiology

Master’s or Ph.D. in Computer Science

Job description

Recruitment Team Lead | Biometrics at Warman O'Brien

Position: Senior/Principal Statistical Programmer | Small CRO | Remote/Hybrid

We are partnered with a small CRO experiencing significant growth within the Biometrics sector.

The Role: As a Senior Statistical Programmer, you will lead high-impact projects, manage complex statistical programming tasks, and oversee project timelines. Your responsibilities include working directly with clients and regulatory agencies to ensure data quality and deliver programming solutions for clinical trials. You will also mentor junior team members, contribute to regulatory submissions, and develop new programming tools.

Key Responsibilities:

1. Lead statistical programming for complex projects, ensuring quality and timely delivery.
2. Collaborate with clients, provide programming oversight, and participate in bid defenses.
3. Contribute to regulatory submissions and represent the company in discussions.
4. Create and validate SDTM and ADaM dataset specifications according to SOPs.
5. Program and validate datasets to ensure accuracy and data integrity.
6. Mentor junior programmers and lead project teams to foster development and collaboration.
7. Develop macros, utilities, and tools to improve efficiency.
8. Implement data integrity checks to ensure scientific accuracy and quality.

Qualifications:

1. Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science.
2. At least 6 years of clinical trial statistical programming experience with a Master’s degree or higher.
3. Experience with clinical trial data, SDTM/ADaM datasets, and regulatory submissions.

Next Steps:

Apply now to seize this opportunity!

Additional Details:

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Analyst and Science
• Industries: Biotechnology Research and Pharmaceutical Manufacturing