Remote Senior Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular, Renal &
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? ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. 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 A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible.
Strong SAS programming experience within the pharmaceutical/CRO industry
Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
Experience supporting regulatory submissions is preferred
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
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 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. If you have the requirements we need, you will be invited for phone interview as the first step. 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 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. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. xehkeey LI-TT1 #LI-Remote #Senior #Contract
Remote working/work at home options are available for this role.
Strong SAS programming experience within the pharmaceutical/CRO industry
Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
Experience supporting regulatory submissions is preferred
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
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 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. If you have the requirements we need, you will be invited for phone interview as the first step. 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 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. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. xehkeey LI-TT1 #LI-Remote #Senior #Contract
Remote working/work at home options are available for this role.