- Home-based remote work opportunities
- Great work/life balance
- Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors
- Cohesive team environment fostering a collaborative approach to study work
- Variety of therapeutic areas, indications and, study phases
- Job stability; long-term engagements and development opportunities
- Technical training and tailored development curriculum
- Career advancement opportunities
- Serves as the primary project team representative, delegating work as appropriate.
- Generates SDTM domains, ADaM data sets, and 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.
- Acts as a liaison between clinical management, subcommittees and project teams as needed.
- May train and mentor new programmers.
- Education/Experience: Minimum bachelor's degree in Statistics, Computer Sciences, Bioinformatics, or related field and 8+ years of hands-on CDISC statistical programming in drug development within the clinical trials industry.
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Statistical Programmer
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Principal Statistical Programmer
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Principal Statistical Programmer - Durham, United States - IQVIA
Description
This position is Full-Time and remote based anywhere in North America
Why 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:
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 $106, $218, 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.
