Clinchoice Inc.
Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)
United States · Principal
Sponsorship not specifiedDetected 26 days ago
Data AnalysisComputer VisionStatisticsStakeholder ManagementClinical TrialsClinical ResearchMedical DevicesSASResearchLeadershipCommunicationBiostatistics
About the role
- 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 Principal Statistical Programmer Consultant to join one of our clients.
Responsibilities
- This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
- Collaborate with Biostatistics, Data Management, and Clinical teams
- Participate in study planning, review specifications, and support submission activities
- The Principal 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.
- Ability to work independently and manage multiple priorities in a fast-paced environment
- Create datasets, tables, listings, and figures according to study requirements
- 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.
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 8 yrs. of clinical programming (CDISC) experience.
- Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Nice to have
- 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
- Experience supporting regulatory submissions is preferred
- Strong communication and stakeholder management skills
Benefits
- Education and Experience:
- ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
Company info
- to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
- 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.
- ClinChoice is an equal opportunity employer.
- We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity.
- Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
Visa & Work Authorization
- 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?
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This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.