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Job Description

Senior/Principal Statistical Programmer, PK/PD

Durham, North Carolina R1444803

Durham, North Carolina| Atlanta, Georgia| Baltimore, Maryland| Charleston, South Carolina| Charlotte, North Carolina| Chicago, Illinois| Cleveland, Ohio| Houston, Texas| Kansas City, Kansas| Kansas City, Missouri| Los Angeles, Kalifornien| Miami, Florida| New Haven, Connecticut| New York City, New York| Orlando, Florida| Overland Park, Kansas| Philadelphia, Pennsylvania| Phoenix, Arizona| Richmond, Virginia| Seattle, Washington| North Carolina| Remote

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Stellenbeschreibung

Work with one of our preferred clients! Our client is a leading pharmaceutical/biotech company dedicated to advancing medical science and improving patient outcomes through the development of innovative therapeutics. Their research-driven organization focuses on discovering, developing, and commercializing novel drugs across various therapeutic areas. We are seeking a highly skilled and motivated Principal Statistical Programmer with expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to join our dynamic FSP team.

Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will play a pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising drug candidates. Leveraging your extensive knowledge of statistical programming and PK/PD principles, you will collaborate closely with cross-functional teams of scientists, clinical researchers, and biostatisticians to ensure the successful implementation of our clinical development programs.

Qualifications:

  • Substantial experience in statistical programming using SAS, R, or other relevant programming languages within the pharmaceutical or biotech industry.
  • Proven expertise in PK/PD data analysis and interpretation, including modeling and simulation.
  • Solid understanding of clinical trial designs, protocols, and regulatory requirements related to PK/PD endpoints.
  • Familiarity with industry standards such as CDISC data structures and guidelines for data submissions.
  • Strong analytical, problem-solving, and communication skills, with the ability to work effectively in cross-functional teams.
  • Detail-oriented with a commitment to producing high-quality deliver
  • Master's or Ph.D. in Biostatistics, Statistics, or a related field with a strong emphasis on pharmacokinetics (PK) and pharmacodynamics (PD) tables within tight timelines.

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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