Job Details

ID #53955357
Estado New Hampshire
Ciudad Livingston
Tipo de trabajo Contract
Salario USD TBD TBD
Fuente Katalyst Healthcares & Life Sciences
Showed 2025-06-02
Fecha 2025-06-02
Fecha tope 2025-08-01
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Clinical Documentation Specialist II

New Hampshire, Livingston 00000 Livingston USA
Aplica ya

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.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.Requirements:Bachelor's degree or international equivalent preferred.Minimum 2 years relevant industry experience in clinical document management or equivalent experience preferred.Demonstrates analytical and critical thinking skills.Excellent oral and written communication skills; ability to facilitate cross-functional team meetings.Demonstrates awareness of clinical documentation business procedures. Compliant to clinical documentation processes.Experienced in using Microsoft PowerPoint and Excel &/or Document Management Systems preferred.

Aplica ya Reportar trabajo