Senior Statistical Programmer, FSP

Durham, North Carolina, United States of America

IQVIA

Solutions to help life sciences organizations drive healthcare forward and get the right treatments to patients, faster.

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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:

  • 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

Job Requirements:

  • Minimum 7 years' experience with Phase I studies, exposure response analysis, cross over design, and supported pooling of PK parameters required
  • Provide hands-on Statistical Programming expertise for client's early phase translation medicine group.
  • Responsible for creating ADaM safety datasets such as ADSL, ADLB, ADVS, ADEX, ADPC (concentration), ADPP (parameter), and POPPK (NONMEM) datasets, PK non-compartmental (NCA) tables, figures, and listings (TFLs).
  • Strong SAS technical skills and in-depth CDISC knowledge required
  • Good knowledge regulatory requirements for submissions
  • Education/Experience: Bachelor’s Degree in Statistics, Computer Sciences, Bioinformatics, or related field, and 7+ years of hands-on experience in Drug Development or clinical trials.

This position is remote based (within United States or Canada) and Full-Time.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

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. https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $106,200.00 - $218,000.00. 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.
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Tags: Bioinformatics CDISC Pharma Research SAS Statistics

Perks/benefits: Career development Health care

Regions: Remote/Anywhere North America
Country: United States

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