AbbVie Associate I, Clinical Documentation in Lake County, Illinois

Associate I, Clinical Documentation


USA, Illinois, Lake County

1 additional location

USA, Illinois

Research & Development

Requisition #1900330

  • 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

Additional Information

  • Travel: No

  • Job Type: Experienced

  • Schedule: Full-time