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Clinical Documentation Associate I

Employer
AbbVie
Location
Lake County, IL, US
Start date
Sep 13, 2019

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Discipline
Clinical, Clinical Documentation
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
BioMidwest, Best Places to Work
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Job Details

  • Active study team member for assigned studies.
  • Ensures real-time inspection readiness of clinical documentation by collaborating with Artifact Owners, reviewing assigned TMFs to ensure accuracy and completeness, and tracking and reporting status to study team(s).
  • Develops and updates study-specific TMF structure documentation.
  • Provides support for audits / inspections.
  • Update CTMS in a contemporaneous manner.
  • Collaborates with CDC Operations colleagues.
  • Complies with GCP, AbbVie SOPs and functional area processes.
  • For assigned countries, may lead and execute study start-up activities including but not limited to:-Prepare submissions to central Ethics Committees. -Review documents and assemble packet required for IP release.


  • Bachelor degree or international equivalent is required
  • Proven analytical and critical thinking skills.
  • Good oral and written communication skills.

Company

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 www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, and YouTube.

Stock Symbol: ABBV

Stock Exchange: NYSE

Company info
Website
Phone
1-800-255-5162
Location
1 North Waukegan Road
 North Chicago
Illinois
60064
US
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