Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Gosford.
This role is for 24 hours per week and is expected to last approximately 1 year.
The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

• Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);
• Planning and coordinating logistical activity for study procedures according to the study protocol
• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Management and shipment of biological samples
• Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
• Administrative research task

We are looking for candidates with:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
• Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
• Good organizational skills with the ability to pay close attention to details

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.co

• Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);
• Planning and coordinating logistical activity for study procedures according to the study protocol
• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Management and shipment of biological samples
• Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
• Administrative research tas