Clinical Document Specialist Intern

Intern, Clinical Document Specialist at Viatris: Ensure quality control of clinical trial documents and support eTMF consistency.

Your Role:

Key responsibilities include:
• Perform quality control of documents submitted to the electronic Trial Master File (eTMF) using established criteria.
• Ensure clinical trial documentation aligns with eTMF specifications, ICH-GCP guidelines, regulatory requirements, and SOPs.
• Monitor and identify study-specific eTMF trends and communicate to the Senior TMF Manager.

About You:

The successful candidate will have:
• Completed a minimum of their second year and be currently enrolled in an accredited college or university in a science/healthcare field or related study.
• A minimum 3.0 GPA is preferred; however, a combination of experience and/or education will be considered.
• Strong organization skills with outstanding attention to detail and follow-through.
• Proficiency in MS Office Suite, specifically in MS Excel and SharePoint.

Compensation & Benefits:
• Viatris offers competitive salaries, benefits, and an inclusive environment.
• The salary range for this position is: $20/hour – $30/hour.

Training & Development:

Opportunities for professional development and mentorship are available to support growth in the healthcare field.

Career Progression:

Potential for career advancement within Viatris, leveraging skills in clinical documentation and trial management.

How to Apply:

Submit your application through the provided link, ensuring all required documents and information are included.

This job may close before the stated closing date, you are encouraged to apply as soon as possible.

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