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Clinical Research Project Coordinator Freelancer

2 tygodni temu

Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

Rho, Inc. is seeking a skilled Clinical Research Project Coordinator Freelancer to join our team as a freelance professional.

Job Summary

The Clinical Research Project Coordinator Freelancer will be responsible for supporting the preparation of Investigator Site Files (ISFs), maintaining the Trial Master File (TMF), and uploading country and site level documents in Veeva Vault. This role requires strong organizational, communication, and teamwork skills, with excellent knowledge of English language.

Key Responsibilities

  • Supports in the preparation of ISFs and TMF.
  • Maintenance of TMF and periodically reviews the TMF to ensure accuracy and completeness.
  • Upload Country and Site level documents in Veeva Vault in a timely manner.
  • Timely transfer of Study documents (scanned copies) to Sponsor, as agreed.
  • Supports in the preparation of documents package for submission to CA and EC, and support for EU CTR submissions.

Requirements

  • Degree in medicine, pharmacy, life science or related field is an advantage.
  • Previous experience in Clinical Trial Assistant or similar role for at least 1 year.
  • Excellent knowledge of English language.
  • Strong organizational, communication and teamwork skills.

What We Offer

  • Competitive salary.
  • Opportunity to learn and grow professionally in Clinical Research field.
  • A job with daily exciting challenges in a highly qualified and international team.
  • Employee-friendly work environment.