Clinical Research Coordinator (Clinical Trials) - Hobart TAS

Location: Hobart, Tasmania, Australia; onsite

Working hours: 24 hours per week; approximately 6 months; immediate start

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Perform prescreening and screening activities and support patient enrollment.
• Maintain study documentation, including protocols, case report forms, consent and privacy records, and EDC systems.
• Coordinate study procedures, patient visits, ECGs, vital signs, potential blood draws, and lab sample processing.
• Enter and verify study data, perform quality checks, and resolve queries.
• Educate patients and communicate with study monitors regarding study-related inquiries.
• Complete general administrative activities required for the clinical trial.

Requirements

• Bachelor’s degree in life sciences or equivalent education and/or relevant clinical or medical experience.
• At least 2 years of experience as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a clinical trial site.
• Understanding of clinical trials and familiarity with study protocols, consent forms, and study schedules.
• Knowledge of medical terminology and strong organizational and interpersonal skills.
• Proficiency in Microsoft Office applications, including Outlook, Word, Excel, and Access.
• Fluent English required.

Culture & Benefits

• Supportive and collaborative work environment.
• Opportunity to contribute to healthcare research and patient outcomes.
• Work with a global team advancing healthcare through data, technology, and human science.