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Intern- Clinical Pharmacology Safety Sciences (Virtual Assignment)

We are currently seeking candidates who are working towards obtaining a MSc or PhD for a virtual internship assignment during the summer of 2021.

Objectives/Goals of the Position:
The intern will compare clinical pharmacology study design, enrollment, regulatory acceptance and total cost across pharmaceutical industry for approved oncology compounds

Primary Responsibilities:  
  • Extract required data for oncology drugs approved between 2003 and 2021 from the sponsor’s FDA/EMA submission package and from other published sources.
  • Analyze collected information to answer stated questions in the proposal including packages at the time of approval and PMC/PMR studies.
  • Prepare a manuscript and submit it to clinical pharmacology journal (e.g. CPT).

Position Requirements:
  • Current enrollment in a US MSc or PhD program.
  • Familiar with clinical pharmacology terms, basic PK/PD and drug-drug interactions knowledge, undertsanding of FDA and EMA guidances related to clinical pharmacolgy.
  • Basic skills in R.
  • Minimum cumulative GPA of 3.0+