Clinical Research Document Specialist

7 days ago


Cork, Cork, Ireland eir evo talent Full time
Job Overview

We are seeking a highly skilled Clinical Research Document Specialist to join our team at eir evo talent. As a key member of our Medical Writing department, you will play a crucial role in the development and delivery of high-quality clinical trial documents.

About the Role

This is an exciting opportunity for a talented Regulatory Content Writer to join our eir evo talent team. You will be responsible for creating comprehensive and scientifically rigorous documents that align with regulatory and ethical standards.

  • Document Development and Writing:
  • Author, review, and finalise high-quality clinical trial documents, including study protocols, initial investigator's brochures, and clinical study reports.
  • Develop and edit manuscripts for publication in peer-reviewed journals, ensuring they meet journal-specific guidelines and uphold the highest standards of scientific integrity.
Key Responsibilities
  • Ensure all documents comply with ICH GCP, regulatory requirements, and internal SOPs.
  • Conduct thorough quality checks to ensure accuracy, consistency, and completeness of data and content.
  • Review and interpret clinical data to ensure accuracy and consistency in documentation, aligning with study objectives and regulatory expectations.


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