Job Overview
This is a unique opportunity to join our global pharmaceutical clients as a Clinical Research Associate.
You will be partnering with one of our global pharmaceutical clients in advancing the development of new medicines, biologic therapies and vaccines for various diseases including cancer, cardio-metabolic diseases, Alzheimer's and infectious diseases.
This role involves site monitoring visits from site selection, RMV to close out, tracking essential documents and liaising with site staff and PI to monitor the progress of assigned trials.
Key Responsibilities
* Site monitoring visits
* Tracking essential documents
* Liaising with site staff and PI
Qualifications
* Tertiary degree qualified in Life Science industry
* 5+ years industry experience with at least 2 years of independent site monitoring experience from CRO/Pharma background
* Oncology experience preferred but not essential
* Excellent communication skills
* Effective time management and organisation skills required to independently manage your workload
Benefits
* Competitive salary
* Annual leave entitlements
* Health insurance offerings
* Retirement planning offerings
* Global Employee Assistance Programme
* Life assurance
* Flexible country-specific optional benefits
About Us
We are dedicated to providing an inclusive and accessible environment for all candidates. We're committed to providing a workplace free of discrimination and harassment.
All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.