Clinical Research Associate Trainee Program Adelaide - Now taking applications for our next intake commencing on the 17th August ****.
Ready to kickstart your career in clinical research? Join IQVIA, a global leader in driving healthcare forward, as a CRA Trainee! We're looking for critical thinking, detail-oriented, and proactive individuals with strong communication skills to join our fantastic CRA Trainee Program in Adelaide.
Applications close Wednesday 13th May ****.
Only applications with full current work rights for Australia can be considered, as we cannot sponsor for this role now, or in the future. Only apply for one location that you wish to be considered for, multiple applications will be rejected. This position is open for Adelaide applications only.
Our Cutting-Edge Training Program
At IQVIA, we're committed to taking clinical research to the next level. Our CRA Training Program is designed with a performance-driven approach, equipping you with the technical and analytical skills to drive healthcare forward. Experience a flexible and engaging curriculum that simulates the life of a CRA, covering all phases of monitoring a clinical trial, including site selection, initiation, monitoring, and close-out. The program also includes:
* Virtual learning activities: Interactive sessions designed to prepare you for real-world scenarios.
* Web-based training: Scenarios and case studies to develop your decision-making skills.
* Learning clinics: Team-oriented learning opportunities to enhance your understanding.
* On-the-job training: Practical experience to build your competence quickly.
* Mentorship: Guidance from experienced professionals to support your development.
What You'll Be Doing
* Participate in a full-time, dedicated training programme covering all aspects of clinical trial monitoring.
* Learn and apply ICH-GCP guidelines, as well as Australian ethical and regulatory requirements.
* Conduct site monitoring visits (under supervision), including selection, initiation, monitoring, and close-out.
* Assist in managing study progress by tracking regulatory submissions, recruitment, and data completion.
* Maintain accurate and organised study documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF).
* Collaborate with study teams and build strong working relationships with sites and colleagues.
What We're Looking For
* A bachelor's degree in a health care or life-science field or equivalent experience.
* Prior experience in a clinical research setting, including roles such as In-house CRA, CTA, or CRC, is advantageous.
* A basic understanding of ICH-GCP and the rules around clinical research in Australia.
* Excellent English communication skills (written and verbal).
* Proficiency in MS Office Suite.
* Strong problem-solving, critical-thinking, and time-management skills.
* Ability to build and maintain positive working relationships.
What To Expect In The Interview Process
You will be asked to complete a pre-recorded video interview and, if successful, may proceed to an assessment interview in person. Video interviews will take place between 6th May to 22nd May ****. If you do not complete your video interview during this time frame, we will not be able to proceed with your application.
Candidates successful for the assessment day in person will be notified by 29th May ****. Interviews will be held in person at the IQVIA offices in early June ****. You must be able to attend during that time frame.
Start date with IQVIA is Monday 17th August ****.
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