
Clinical Trial Assistant
15 hours ago
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.
- 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).
- Entry level
- Full-time
- Research
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