Senior Statistical Programmer/Analyst Consultant - (remote in US)

Clinchoice; New York (NY); Remote; USD 120,000 - 180,000; Full time

Job summary

ClinChoice is seeking a Senior Statistical Programmer Consultant to join a client-facing project within our global CRO environment. The role emphasizes independent work under a Programming team lead, delivering high-quality programming components for clinical studies.

The ideal candidate has 5+ years of CDISC programming experience, strong SAS skills, and a solid understanding of ICH/GCP. This position offers career development and exposure to large, cross-functional teams across regions.

Qualifications

• Bachelor's or higher in CS, statistics, or related science.
• 5+ years clinical programming (CDISC) for Bachelor's; 6+ years for Master's.
• Strong knowledge of ICH/GCP and clinical development processes.
• Excellent written and verbal communication; able to coordinate with study teams.

Responsibilities

• Lead and/or support programming deliveries for a clinical study or project.
• Implement statistical programming aspects of the protocol and development program.
• Ensure high quality of deliverables and documentation; write specifications.
• Develop best practices to improve quality, efficiency, and automation usage.
• Communicate risks and align with study team members.

Skills

CDISC programming

Clinical programming

Statistical programming

ICH/GCP knowledge

Communication skills

Education

Bachelor's degree in CS/Statistics

Master's degree in CS/Statistics

Tools

SAS

CDISC SDTM/ADaM

Job description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds.... ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client's counterparts.

Main Job Tasks and Responsibilities

The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks

Key Responsibilities

• Responsible for supporting the Programming deliveries of a clinical study or project.
• Implements statistical programming aspects of the protocol and the clinical development program.
• Ensures high quality is built into own deliverables and the quality delivered by other programmers.
• Programs independently with high efficiency and quality.
• Writes and/or implements specifications and oversees completeness of relevant documentation.
• Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.
• Ensures compliance with standards and automation usage.
• Plans and support team activities and tasks.
• Communicates and escalates risks within the assigned studies and/or projects.
• Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.

Education and Experience

• Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience.
• Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
• Good understanding of the clinical drug development process.
• Strong communication skills and coordination skills.
• Current knowledge of technical and regulatory requirements relevant for the role
• Ability to proactively manage concurrent activities within a project
• Proficient ability to influence relevant stakeholders on programming-related items

Who will you be working for?

About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel.