Clinical Trial Administrator-FSP

3 weeks ago


North Ryde, New South Wales, Australia Parexel Full time

Clinical Study Support

At Parexel, we strive to achieve excellence in our clinical trials. As a Clinical Trial Administrator-FSP, you will play a crucial role in ensuring the successful and timely completion of all clinical trial milestones.

Your Responsibilities:

  • Assist the CO team with in-house activities and documentation associated with the set up and management of trial activities.
  • Coordinate translations of documents after review/translation and submit for TMF filing.
  • Support the CRA to prepare the safety information submission per site-specific requirement.
  • Create and update the ISF, including paper ISF and binders.
  • Support study routine supplies purchase, distribution, calibration validity of loaned equipment.
  • Assist in organization and execution of investigator meeting.
  • Maintain study information in CTMS on behalf of the Clinical Trial Manager.

Central Administrative Support

As a Clinical Trial Administrator-FSP, you will also provide logistic support, organization to CO internal and external meetings, trainings.

Requirements:

  • Bachelor's degree in a related field.
  • Good organizational and communication skills.
  • Well-understood Good Clinical Practice, ICH-GCP.
  • Command of Microsoft Office applications.
  • Ability to work as a team and backup team members.
  • Minimum 1 year of working experience in the pharma industry or related industry.


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