Clinical Trial Coordinator
4 days ago
Job Summary
Clinical Trials Nurse required for a pharmaceutical company sponsored clinical trials for a private site
-KEY Responsibilities
- Coordinate and support all operational aspects of clinical trials according to GCP, regulatory requirements, and protocol guidelines.
- Assist in the preparation, submission, and maintenance of regulatory documentation (e.g., IRB submissions, informed consent forms).
- Schedule and oversee study visits, monitor subject enrollment, and maintain communication with investigators, site staff, and sponsors.
- Ensure timely data entry, query resolution, and accurate documentation in electronic data capture systems.
- Monitor inventory and handling of study supplies, investigational products, and trial-related documents.
- Collaborate with cross-functional teams including regulatory, medical, and data management.
- Participate in site monitoring visits, audits, and inspections as needed
Qualifications
- Degree in nursing with AHPRA registration is a preference
- Bachelor's degree in life sciences, healthcare, or related field with experience in Clinical Trials
- 1–3 years of experience in clinical research or clinical trial coordination preferred.
- Knowledge of GCP, ICH guidelines, and FDA regulations.
- Strong organizational skills and attention to detail.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).
Job Type: Full-time
Pay: $35.00 – $42.00 per hour
Work Authorisation:
- Australia (Required)
Work Location: In person
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