Principal Statistical Programmer - FSP
Senior or Principal Statistical ProgrammerWhy DSSS?Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership.
This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems.
These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work within an eco-system where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies.
With IQVIA's DSSS business unit, you are not just another cog in the machine; you become a core part of a dynamic team dedicated to reshaping the future of healthcare.
Additional
Benefits:
Home-based remote work opportunitiesGreat work/life balanceCollaborate on projects and innovations with industry leaders in the Pharma and CRO sectors Cohesive team environment fostering a collaborative approach to study workVariety of therapeutic areas, indications and, study phasesJob stability; long-term engagements and development opportunitiesTechnical training and tailored development curriculumCareer advancement opportunitiesJob Requirements:
Generates SDTM domains, ADaM datasets, and Define.
xml files with proficiency in creating specification files for these domains.
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data.
Reviews output across programs to ensure consistency.
Reviews maintains and approves study documents per standard procedures.
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures.
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting.
Participates in the development and/or maintenance of departmental procedures and standards.
Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures.
Implements data management plans designed to meet project and protocol deadlines.
Education/
Experience:
Minimum bachelor s degree in Statistics, Computer Sciences, Bioinformatics, or related field PLUS 8
years of clinical trials industry experience.
This position is Full-Time and remote based anywhere in the United Sates or CanadaIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.
The potential base pay range for this role, when annualized, is $111,400.
00 - $203,100.
00.
The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
SummaryLocation:
Durham, North Carolina, United States of AmericaType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems.
These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work within an eco-system where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies.
With IQVIA's DSSS business unit, you are not just another cog in the machine; you become a core part of a dynamic team dedicated to reshaping the future of healthcare.
Additional
Benefits:
Home-based remote work opportunitiesGreat work/life balanceCollaborate on projects and innovations with industry leaders in the Pharma and CRO sectors Cohesive team environment fostering a collaborative approach to study workVariety of therapeutic areas, indications and, study phasesJob stability; long-term engagements and development opportunitiesTechnical training and tailored development curriculumCareer advancement opportunitiesJob Requirements:
Generates SDTM domains, ADaM datasets, and Define.
xml files with proficiency in creating specification files for these domains.
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data.
Reviews output across programs to ensure consistency.
Reviews maintains and approves study documents per standard procedures.
Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.
Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures.
Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting.
Participates in the development and/or maintenance of departmental procedures and standards.
Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures.
Implements data management plans designed to meet project and protocol deadlines.
Education/
Experience:
Minimum bachelor s degree in Statistics, Computer Sciences, Bioinformatics, or related field PLUS 8
years of clinical trials industry experience.
This position is Full-Time and remote based anywhere in the United Sates or CanadaIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.
The potential base pay range for this role, when annualized, is $111,400.
00 - $203,100.
00.
The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
SummaryLocation:
Durham, North Carolina, United States of AmericaType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
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