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Senior Associate, Clinical Pharmacology Scientific Support & Reporting

AbbVie
North Chicago, United Statesfull_timeVerifiedPosted 18 Mar 2025

About the role

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose:

To build all necessary data / information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.

Description:

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
  • Review clinical protocols and key decisions impacting project timelines with management.
  • Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies.
  • Apply experience to analyze clinical study data, including statistical data using available soft ware to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
  • Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timeline with minimal supervision
  • Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
  • Integrate clinical trial data across studies and identify issues impacting projects and provide this information to internal peers and therapeutic area management.
  • Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
  • Participate on teams for process improvement initiatives

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Company

AbbVie

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