Clinical Documentation Specialist

Spectraforce Technologies
United States, Illinois, North Chicago
Oct 28, 2024
Job Title: Clinical Documentation Specialist Duration: 12 months Location: 100% Remote Major Responsibilities: Manage Phase I to IV study activities. Ensures the Master File is always inspection-ready and complies with ICH GCP guidelines. This role involves regularly updating and assisting study teams to address issues related to key Master File health indicators, including the completeness, accuracy, and timeliness of all essential documents throughout the lifecycle of assigned clinical trials. Ensured the Master File was always inspection-ready and complied with ICH GCP guidelines. This role involves regularly updating and assisting study teams to address issues related to key Master File health indicators, including the completeness, accuracy, and timeliness of all essential documents throughout the lifecycle of assigned clinical trials. 1. Bachelor's degree or international equivalent preferred. Minimum 2 years relevant industry experience in clinical document management or equivalent experience preferred. 2. Demonstrates analytical and critical thinking skills. 3. Excellent oral and written communication skills; ability to facilitate cross-functional team meetings. 4. Demonstrates awareness of clinical documentation business procedures. Compliant to clinical documentation processes 5. Experienced in using Microsoft PowerPoint and Excel &/or Document Management Systems preferred.