Principal PKPD/NONMEM Programmer - R Programming

Posted 6 Days Ago
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6 Locations
In-Office or Remote
Senior level
Software • Analytics • Biotech
The Role
The role involves programming and quality control of NONMEM PK/PD datasets, ensuring data accuracy, communication with departments, and QC of R packages.
Summary Generated by Built In

Deliverables: 
•    Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc. 
•    Clear communication with partnering departments: Data Management, Statistics, Statistical Programming and Bio-analytical providers.
•    Ensures quality NONMEM input data (accurate, valid and complete) is provided to the Pharmacometrics Leaders within projected timelines for low to medium complexity projects.
•    Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements.
  

Responsibilities

•    Programming and QC of NONMEM PK/PD datasets based on SDTM/ADAM datasets. 
•    Follow up and QC of outsourced NONMEM datasets.  
•    Prepare submission projects per internal PM guideline.
•    QC of existing, customized R packages used for standardization of Pharmacometric works (build testing suite of customized packages).

Top Skills

Nonmem
R
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The Company
HQ: Waltham, MA
1,395 Employees
Year Founded: 1987

What We Do

Cytel enables decision-makers in the life sciences to unlock the full potential of their products. From navigating uncertainty to proving value, Cytel’s 30 years of global expertise in consulting, data-driven analytics, and industry-leading software helps biotech and pharmaceutical companies transform intelligence into confident decisions. We have an uncompromising commitment to scientific rigor and high standards of operational excellence, which are channeled through our locations in North America, Europe, the United Kingdom, and Asia. Together, we enable our clients to deliver the therapies that propel humanity forward. Cytel employs a range of data science tools from biostatistics to machine learning to help executives in the life-sciences to make confident decisions powered by data. We are probably best known for being leaders in the field of adaptive clinical trial design, a subset of trial design that uses interim looks to enhance the patient safety and commercial value of pharmaceutical products. We also have specialists in Bayesian statistics, real world evidence, artificial intelligence, health economics, and a number of other research fields to ensure that academic and scientific findings can have impact on industry quickly and seamlessly. www.cytel.com

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