Senior Statistical Programmer Consultant - Client-Facing

ClinChoice; United States; On-site; USD 120,000 - 170,000; Full time

Job summary

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client teams. This delivery-focused role leads and supports programming efforts to deliver statistical programming components of a clinical project.

The ideal candidate will have CDISC experience, strong communication and collaboration skills, and the ability to manage concurrent activities across a study team in a fast-paced CRO environment.

Qualifications

• CDISC experience and ICH/GCP familiarity.
• Strong communication and coordination abilities.
• Ability to manage concurrent activities in a project.
• Proficiency in regulatory terminology and clinical trial processes.
• Experience collaborating with statisticians, lead programmers, and data managers.

Responsibilities

• Support programming deliveries for a clinical study or project.
• Implement statistical programming aspects of the protocol and development program.
• Ensure high quality in own deliverables and in others’ work.
• Program independently with accuracy and efficiency.
• Write specifications and oversee documentation completeness.
• Contribute to best practices to improve quality and efficiency.
• Ensure compliance with standards and automation usage.
• Plan and support team activities and tasks.
• Communicate and escalate risks within studies/projects.
• Collaborate with study team members (Statistician, Lead Programmer, Data Manager, Study Leader).

Skills

CDISC experience

Communication skills

Coordination skills

Regulatory knowledge

Project management

Stakeholder influence

Education

Bachelor’s degree in CS or statistics or related field

Master’s degree in CS or statistics or related field

Job description

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client teams. This delivery-focused role leads and supports programming efforts to deliver statistical programming components of a clinical project.

The ideal candidate will have CDISC experience, strong communication and collaboration skills, and the ability to manage concurrent activities across a study team in a fast-paced CRO environment.