Clinical Trial Assistant

3 weeks ago

Sydney, New South Wales, Australia Canopy Clinical Research Full time
Overview

Direct message the job poster from Canopy Clinical Research

Closing patient access gaps in clinical research. We have an exciting opportunity to join a collaborative team of Clinical Research professionals focused on improving patient outcomes through Phase I to IV clinical trials in our Sutherland Shire site.

We are seeking a dynamic Clinical Trials Assistant with a passion for improving health who is able to support the Clinical Trials Site team and who has the ability to take initiative and help the team where required.

Responsibilities
  • Work closely within a multidisciplinary team of Clinical Research professionals including Trial Coordinators, Nurses, Phlebotomists, Lab Technicians, Doctors and the Site Director.
  • Work under the supervision of the CRC and Site Director with administrative tasks including data entry.
  • Act as the unblinded checker for trial activities as part of the unblinded team.
  • Support and backfill into the laboratory technician role under the guidance of a Senior Laboratory Technician.
  • Support the Trial Study team with distribution of site materials and equipment as required.
  • Collection of data in accordance with GCP standards within the scope of your role.
  • Provide administrative support for site meetings if required.
  • Setup and maintain trial information on site CTMS, as well as physical trial documentation collection and quality checks, within the scope of your role.
  • Assist with other duties as required, e.g. clinical trial stock management, calibration, equipment checks.
  • Remotely support other sites with eCRF data entry if required.
About you
  • Previous experience as a Clinical Trials Assistant within the pharmaceutical or biotechnology industry or at an investigative site is highly desired.
  • Degree in science or medical qualification such as Biomedical Science or Medical Science or equivalent work experience.
  • Ability to work independently with a high level of initiative; also able to work as part of a team.
  • Basic knowledge and understanding of Essential Documents, CFR and GCP/ICH.
  • Proficiency with learning and understanding technological systems (Microsoft Office, TMF, CTMS).
  • Strong administration skills with high attention to detail.
  • Excellent interpersonal, verbal and written communication skills.
  • Team player with a positive, can-do attitude.
  • Basic knowledge about clinical research processes.
  • ICH-GCP training and certification (can complete this on the job).
Seniority level
  • Entry level
Employment type
  • Full-time
Industries
  • Research

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