Clinical Trials Phlebotomist: Fast-Paced Team Impact

Canopy Clinical Research

Northern Beaches Council

On-site

AUD 60,000 - 75,000

Full time

11 days ago
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Job summary

Canopy Clinical Research in Brookvale, NSW is seeking an experienced phlebotomist to join a collaborative team of clinical trials professionals focused on advancing patient outcomes from Phase I to IV.

The role includes phlebotomy, data entry, site file management, and supporting trial coordinators to keep study timelines and quality. You'll work in a fast-paced environment with opportunities to grow in clinical trials while maintaining participant safety.

Qualifications

  • Certificate III in Pathology Collections is required.
  • Degree in science or medical qualification such as Biomedical Science or Medical Science.
  • Previous phlebotomy experience and ICH/GCP familiarity are advantageous.

Responsibilities

  • Provide clinical trial administrative and operational support within a multidisciplinary team.
  • Perform venepuncture and specimen processing, packaging and shipping per protocol.
  • Maintain Investigator Site File with required documents and quality review.
  • Accurate data entry into the clinical trial database and monitor query resolution.
  • Support study status reports and trial coordination activities as needed.
  • Manage trial inventory and supply ordering; assist with site meetings.
  • Use EMR and CTMS for trial information and assist unblinded pharmacy teams.

Skills

Phlebotomy
Administrative skills
Data entry
Team player

Education

Certificate III in Pathology Collections
Degree in science or medical qualification such as Biomedical Science or Medical Science

Tools

Microsoft Office
TMF
CTMS

Job description

Canopy Clinical Research in Brookvale, NSW is seeking an experienced phlebotomist to join a collaborative team of clinical trials professionals focused on advancing patient outcomes from Phase I to IV.

The role includes phlebotomy, data entry, site file management, and supporting trial coordinators to keep study timelines and quality. You'll work in a fast-paced environment with opportunities to grow in clinical trials while maintaining participant safety.

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