R Programmer, PKPD

This position is Full-Time and home-based in the United States or Canada. East coast strongly preferred.

Why IQVIA

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 CRO while operating within a sponsor environment and utilizing sponsor systems. Being part of DSS means being part of a passionate team dedicated to advancing medicine and reshaping healthcare. Your role will be both challenging and rewarding, making a real impact.

Experience the best of both worlds and become a core part of our dynamic team today!

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
• Career advancement opportunities

Responsibilities:

• Conduct analysis of clinical pharmacokinetic/pharmacodynamic (PK/PD) data using R.
• Combine, manipulate, transform, and summarize data; processes data iteratively.
• Data visualizations and dynamic documents.
• Develop standardized programs to automate reports and graphs.
• Create and/or validate clinical PK/PD study output and requirements consistent with data definitions, specifications, and relevant study documentation (e.g. protocol, SAP, aCRF), including ADHOC and interim analysis requests. For example, analysis/modeling as required for dose tolerance, dose proportionality, bioavailability, and drug-drug interactions, as well as population PK studies.
• Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group.
  

Qualifications:

• Bachelor’s degree in Math, Stats, Computer Science or similar, plus 4 years’ experience programming within the pharmaceutical/clinical trial/CRO industry
• Advanced R programming plus recent PK/PD experience required
• Desire to work in clinical PK/PD – knowledge and experience of PK/PD concepts and related programming is desirable, but not required.
• Experience visualizing/presenting data for internal stakeholders or clients
• Capable of implementing more advanced modeling and statistical procedures as requested by study team.
• Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis, and reporting/modeling of analysis results. Including handling of data issues and uncleaned data.
• Knowledge of CDISC standards (SEND, SDTM, and ADaM) is desirable.

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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

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $65,000.00 - $108,300.00. 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.