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.
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Job Description
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.
Significant Work Activities -Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Qualifications
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.
Additional Information
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.
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