Principal Document Specialist

hace 1 semana


Xico, México Worldwide Clinical Trials A tiempo completo
Job Description:

We are seeking a skilled professional to support the processing, maintenance, and archiving of essential documents in compliance with industry standards. Key responsibilities include performing lead activities, supporting setup, maintaining resources, and providing subject matter expert support.

About Worldwide Clinical Trials:
Worldwide Clinical Trials is committed to enabling professionals from all backgrounds to succeed and thrive in their roles. Our diverse and inclusive environment promotes collaboration and creativity.

Key Responsibilities:
  • Perform RMC lead activities
  • Support TMF setup
  • Maintain Sciforma resources
  • Provide subject matter expert support

Requirements:
  • Data collection, indexing, and editing skills
  • Excellent written and verbal communication skills
  • Strong interpersonal skills

Preferred Qualifications:
A university degree in a life science is preferred. Up to 1-2 years of relevant experience is required.

Benefits:
We prioritize a diverse and inclusive environment that promotes collaboration and creativity. We offer a competitive salary and benefits package, estimated to be around $80,000 - $100,000 per year.

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