Clinical Research Coordinator part time - Perth WA

Are you looking for an opportunity or a new challenge in Clinical Research? Do you want to work for an industry leading company?

IQVIA is currently recruiting for a Clinical Research Coordinator to work at our site in Spearwood WA to support conducting a clinical trial.

- Part time: 24h per week

- Duration: asap for 5 months

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

• Perform a variety of complex clinical research procedures including but not limited to electrocardiogram (ECG), lab sample collection, blood draw etc

• Handles lab testing and analysis including preparation of specimen collection tubes and lab logistics

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator

• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns

• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents

• Plan and coordinate logistical activity for study procedures according to the study protocol

• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues

• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol

• Correct custody of study drug according to site standard operating procedures

• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• 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, nurse, medical assistant, other medical profession 

• Experience working on clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

• Experience in respiratory

• Skill in carrying out required clinical procedures including phlebotomy and ECG

• Phlebotomy certification

• 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 client

• ​Good organizational skills with the ability to pay close attention to detail.

• Valid working rights for Australia

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com