Unknown - Senior Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)
Requirements
• 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. • Need to have Respiratory/Immunology TA experience. • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology. • The Application Process • Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. • Who will you be working for? • 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 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. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
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 • Senior Statistical Programmer Consultant • Key Requirement: • Key Requirement: • Strong SAS programming experience within the pharmaceutical/CRO industry • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies • Experience in generating and validating SDTM, ADaM, and TLFs • Good understanding of CDISC standards and clinical trial processes • Ability to work independently and manage multiple priorities in a fast-paced environment • Experience supporting regulatory submissions is preferred • Strong communication and stakeholder management skills • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting • Create datasets, tables, listings, and figures according to study requirements • Collaborate with Biostatistics, Data Management, and Clinical teams • Ensure programming deliverables meet quality standards and project timelines • Participate in study planning, review specifications, and support submission activities
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