Skip to main content

This job has expired

You will need to login before you can apply for a job.

Associate II, Clinical Pharmacology Scientific Support & Reporting (On-Site, IL Based)

Lake County, Illinois
Start date
Feb 20, 2024

Job Details

This position will be required to be on-site 3 days / week from our Lake County, IL office

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Reviews clinical protocols and coordinate advisory meeting agendas, activities, slide decks and consulting agreements
  • Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.
  • Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews.
  • Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
  • Integrate clinical trial data across studies, identify issues impacting projects and provide the relevant information to internal peers and therapeutic area management.
  • Perform literature and competitive intelligence searches
  • Responsible for receiving and completing tasks and assignments from function or Therapeutic Area MD or Scientific Staff within timeline with minimal supervision
  • Appropriate and effective use of resources to complete tasks and meet required timelines.
  • Responsible for maximizing individual, function/therapeutic area and team productivity; and mentor function/therapeutic area personnel.

  • Bachelors/Master’s degree, in Science related to Field, with +5 years’ experience in pharmaceutical industry
  • Associates degree/RN with 9+ years of experience in pharmaceutical industry may be additionally considered
  • Understanding of basic clinical study principles
  • Must possess good oral and written communication skills
  • Proficient in using computer to analyze clinical study data, generate reports and create presentations
  • Experience supporting clinical research, drug development and/or function/therapeutic area operations.
  • Must have proven record of successful projects.
  • Must be able to produce work of highest quality by paying attention to detail
  • Ability to identify opportunities and participate in process improvement initiatives.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.


AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, and YouTube.

Stock Symbol: ABBV

Stock Exchange: NYSE

Company info
1 North Waukegan Road
North Chicago

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert