This is an exciting opportunity for an experienced Clinical Research Associate to join a private, full-service contract research organisation. The Clinical Research Associate is primarily responsible for the implementation and conduct of global or local Phase 1 - 4 clinical studies according to local regulatory requirements, policies and guidelines and in line with ICH GCP.
As CRA with this rapidly growing organisation you will be responsible for monitoring local and international clinical studies. As a key member of this entrepreneurial and fast-paced team you will focus on data integrity and patient safety in accordance with specific country regulations as well as plan day to day activities for monitoring clinical studies to ensure the accurate and timely submission of monitoring reports.
To be successful in this role you will be degree qualified in clinical science or a health related field or are a licensed health-care professional. You will have experience in monitoring complex and global trials ideally with a CRO background. Also required for this role is an attention to detail, the ability to work simultaneously on multiple priorities and the ability to travel locally or internationally.
If you are a CRA who thrives on being an integral part of the clinical team and are looking for opportunities for expedited promotion to the role of a senior CRA and subsequent Project Management then this role is for you. To apply for this role please submit your cv together with a covering letter to email@example.com
|Expertise Area||Clinical Research|
|Advertising Organisation||Heat HR Consulting|
|Link to Website||heathrconsulting.com.au|
|Contact Name||Linda Lyons|
|Phone||0413 317 640|
|Last Date of Applications||Wednesday, 8th of March 2017|