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Job Description

Principal Statistical Programmer, Early Phase (PK/PD) - FSP

Reading, United Kingdom Full time R1408700

Reading, United Kingdom| Netherlands| Denmark| Germany| Spain| Poland| Belgium| United Kingdom| Remote

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Job Description

Why  IQVIA 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.

Job Requirements:

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).
Experience with Phase I studies, exposure response analysis, cross over design, and supported pooling of PK parameters required
Strong SAS technical skills and in-depth CDISC knowledge
Good knowledge regulatory requirements for submissions
Project/Study lead experience strongly preferred

Education/Experience:  

5+ years of Statistical Programming experience in CRO/Pharmaceutical industry.

  • Strong exposure/experience in early phase studies.

  • CDISC (SDTM, ADaM, and TLF’s) experience.

  • Strong PK/PD experience in CDISC including PC, PP, ADPC, and ADPP.

  • Experience in NONMEM Dataset creation and analysis.

  • Good hands-on experience in SAS.

This position is remote based (Anywhere in Europe) and Full-Time.

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

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

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