As a Clinical Research Associate, you will collaborate with pharmaceutical clients to advance the development of medicines, therapies, and vaccines for challenging diseases.
Key Responsibilities:
* Conduct site monitoring visits from selection to close out
* Track essential documents and liaise with site staff and Principal Investigators (PI) to monitor trial progress
* Collaborate with cross-functional teams embedded within a single sponsor organisation
* Elevate any protocol deviations or risk of delays to study milestones to the Clinical Trial Manager and collaborate with stakeholders
Requirements:
* Tertiary degree qualified in Life Sciences
* Minimum 5 years industry experience with at least 2 years independent site monitoring experience from CRO/Pharma background
* Oncology experience preferred but not essential
* Excellent communication and organisational skills required to manage workload independently