Clinical Pharmacology Support Associate II

1 week ago


North Chicago Illinois, United States AbbVie Full time
Position Overview:

The role involves the compilation of essential data and information required for the development of internal documents and scientific reports pertinent to clinical trials. This position demands the ability to manage multiple reports concurrently through effective multi-tasking.


Key Responsibilities:
  • Draft scientific reports and presentations related to clinical trials utilizing available software and established templates.
  • Responsible for authoring basic protocols and clinical study reports.
  • Adhere to procedures outlined in relevant IQS documents, study protocols, and directives from management concerning clinical studies.
  • Leverage experience to analyze clinical study data, including statistical information, using available software to support ongoing blinded/un-blinded pharmacokinetics, safety, and efficacy evaluations.
  • Receive and execute tasks and assignments from the function or Therapeutic Area Medical Director or Scientific Staff within designated timelines and with minimal oversight.
  • Conduct literature reviews and competitive intelligence searches.
  • Ensure the scientific integrity of all processes by consistently applying current electronic document conventions and processes accurately.
  • Integrate clinical trial data across various studies, identify issues affecting projects, and provide pertinent information to internal colleagues and therapeutic area management.
  • Utilize resources effectively to complete tasks and meet required timelines.
  • Enhance individual, function/therapeutic area, and team productivity; mentor personnel within the function/therapeutic area.


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