Senior Statistical Programmer/Analyst Consultant

🔥 4 minutes ago

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟠 Senior

🖥 Software Engineer

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👻 Ghost score 10%

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• Support programming deliveries of a clinical study or project • Implement statistical programming aspects of the protocol and clinical development program • Ensure high quality in own deliverables and work delivered by other programmers • Program independently with high efficiency and quality • Write and/or implement specifications and oversee completeness of relevant documentation • Contribute to best practices improving quality, efficiency, and effectiveness within the function • Ensure compliance with standards and automation usage • Plan and support team activities and tasks • Communicate and escalate risks within assigned studies and/or projects • Work proactively with study team members, including the Statistician, Lead Programmer, Data Manager, and Study Leader • Work under the leadership, oversight, and direction of a Programming team leader

🎯 Requirements

• Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; or 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 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 • High technical skills and thorough industry knowledge • Ability to work independently in a client-facing role • Ability to establish a high-trust environment with client counterparts

🏖️ Benefits

• Professional development • Continuous training • Supportive culture • Equal opportunity and diversity/inclusivity • Career opportunities associated with working for a global CRO