Associate I, Clinical Documentation
- Employer
- AbbVie
- Location
- Lake County, IL, US
- Start date
- Jan 14, 2019
View more
- 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.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled
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
- http://www.abbvie.com/
- Phone
- 1-800-255-5162
- Location
-
1 North Waukegan Road
North Chicago
Illinois
60064
US
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