Description:
Position Title: Clinical Documentation Specialist II
Length of Contract: 1 year
Location/Site: Lake County - North Chicago - Hybrid Preferred
What are the top 3-5 skills, experience or education required for this position:
1. Ability to actively engage with document owner to ensure study team members are accountable for their respective sections of the Master file.
2. Work collaboratively with document owners and cross-functional teams to resolve document-related issues.
3. Analytical and critical thinking skills.
4. Continuously monitor TMF Health metrics to detect any trends, identify potential risks and implement mitigation strategies to ensure document integrity and compliance.
5. Excellent organizational skills with ability to manage several studies at the same time.
Purpose :
The Clinical Document Management Associate II will ensure the Master File is always inspection-ready and
complies with ICH GCP guidelines. This role entails the conduct of rigorous quality checks, ensuring reliable
and complete Trial Master File. Collaborate with study teams, providing support to address and resolve issues
related to Master File health indicators. Focus on maintaining the completeness, accuracy, and timeliness of
all crucial documents throughout the lifecycle of the assigned clinical trials.
Responsibilities :
Qualifications
Provide the days of the week and the hours that this position will require:
Additional Details
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