Clinical Trials Coordinator

15 hours ago


Hobart, Tasmania, Australia Pharmiweb Full time
About this role

We are seeking a highly skilled Clinical Trials Coordinator to join our team in Germany.

The successful candidate will be responsible for ensuring data integrity, quality, and compliance with ICH GCP and local requirements at the site level.

Key Responsibilities
  • Conduct monitoring activities using different methods, including on-site and remote visits
  • Review source documents and verify accuracy of clinical data entered in the Case Report Form (CRF)
  • Manage reporting of protocol deviations and follow up on queries
  • Verify Investigational Product (IP) inventory and reconcile discrepancies
  • Ensure all activities are managed by site personnel who are appropriately delegated and trained
Requirements
  • Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
  • Advanced level or fluency in English is required; proficiency in local language is also necessary
  • Excellent communication, presentation, and interpersonal skills
  • Ability to adapt to changing technologies and processes
Compensation

The estimated salary for this role is €55,000 - €65,000 per annum, depending on experience.

About Pharmiweb

We support clinical studies across various therapeutic areas and have longstanding partnerships with a vast client base.



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