Clinical Research Associate

6 months ago

Sydney, Australia IQVIA Full time

**IQVIA Australia**

Australia is known globally as one of the world’s most diverse and welcoming countries. There are more than 500 national parks and bustling cities on the biggest island in the world.

**What is in it for you?**

A competitive base salary, generous car allowance, additional health allowance, annual bonus, flexible working, lifestyle, picnic and community days. You will have the opportunity to build a career in a supportive environment, work with Industry leading Pharmaceutical companies and inspiring thought leaders. We celebrate your success, we celebrate our learnings, we celebrate Healthcare. This is just the beginning.

**Key Responsibilities**
- Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas
- Administer protocol and related study training to assigned sites and establish regular lines of communication
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
- Collaborate and liaise with study team members for project execution support as appropriate.

**Not everyone can be a CRA it’s an extraordinary role, do you meet this unique criteria?**
- Bachelor's degree in Life Sciences or other scientific/nursing disciplines is essential
- Minimum of 2 years independent site monitoring experience
- CRO experience is highly desired
- Ability to travel on a regular basis which will involve interstate travel
- Extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is required

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