Part-Time Clinical Research Coordinator — 8-Month Trial

QPL IQVIA RDS Poland Sp. z o.o.; North Sydney; On-site; AUD 70,000 - 90,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to support a site in Macquarie Park. This role is 24 hours per week with some shift and Saturday work, starting immediately for approximately 8 months.

You will perform a range of administrative and clinical support tasks, including prescreening, chart reviews, study documentation, patient enrollment, IP/site accountability, data management in EDC/IRTs, and liaison with monitors to keep trials compliant and on schedule.

Qualifications

• Bachelor’s degree in life sciences or equivalent education.
• Experience in clinical trials or site-based coordination.
• Knowledge of study protocols, consent forms, and schedules.
• Familiarity with IRT/IWRS systems and lab sample handling.

Responsibilities

• Prescreening and Screening tasks
• Review charts from the site data base
• Maintaining and updating study documentation, including protocols, CRFs, EDC systems and eTMFs
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• IP - site accountability including IP - patient compliance
• Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
• Processing and shipment of lab samples process
• Patient scheduling support
• Printing and certifying EMR
• Coordinating logistical activities for study procedures in line with the study protocol
• Communicating with study monitors and responding to study-related inquiries
• Carrying out general administrative tasks related to the study

Skills

Interpersonal communication

Attention to detail

Organizational skills

MS Office proficiency (Outlook, Word,

Education

Bachelor’s degree in life sciences

Tools

IRT/IWRS systems

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to support a site in Macquarie Park. This role is 24 hours per week with some shift and Saturday work, starting immediately for approximately 8 months.

You will perform a range of administrative and clinical support tasks, including prescreening, chart reviews, study documentation, patient enrollment, IP/site accountability, data management in EDC/IRTs, and liaison with monitors to keep trials compliant and on schedule.