Overview
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Blacktown. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Responsibilities
* Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
* Supporting patient screening and enrollment, including handling informed consent and privacy documentation
* Coordinating logistical activities for study procedures in line with the study protocol
* Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
* Managing and shipping biological samples
* Communicating with study monitors and responding to study-related inquiries
* Help with patient recruitment, patient education and community outreach
* Carrying out general administrative tasks related to the study
Qualifications
* Bachelor's degree in life sciences or equivalent education and / or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
* Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
* Good knowledge of medical terminology
* Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
* Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
* Excellent interpersonal and communication skills
* Strong organizational skills and attention to detail
#J-18808-Ljbffr