Clinical Research Associate Trainee Program (Sydney)

IQVIA; North Sydney; On-site; AUD 60,000 - 80,000; Full time

Job summary

IQVIA is offering a Clinical Research Associate Trainee Program in Sydney. The program combines classroom learning with hands-on CRA experiences, guided by senior CRAs, Line Managers, and Quality Managers.

On graduation, trainees join IQVIA as CRAs in either the Full Service or Flexible Resource model, with clear career progression paths toward senior CRA or project management roles. Applicants should hold a health-science bachelor’s degree or equivalent, have strong communication skills, and a

Qualifications

• Bachelor's degree in health care or life-science required or equivalent experience.
• Basic understanding of ICH-GCP and Australian clinical research rules.
• Excellent English communication skills (written and verbal).
• Proficiency in MS Office Suite.
• Strong problem-solving, critical thinking and time management skills.

Responsibilities

• Participate in a full-time training program covering all aspects of clinical trial monitoring.
• Learn and apply ICH-GCP guidelines and Australian regulatory requirements.
• Conduct site monitoring visits under supervision (initiation, monitoring, close-out).
• Assist in tracking regulatory submissions, recruitment and data completion.

Skills

Critical thinking

Attention to detail

English communication

MS Office

Time management

Relationship building

Education

Bachelor's degree in health care or life-science

Tools

MS Office Suite

Job description

Clinical Research Associate Trainee Program

Sydney- Now taking applications for our next intake commencing on the 1st February 2027.

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 Sydney.

Applications close Sunday 18th October 2026.

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 Sydney applications only.

This is your chance to gain the skills and knowledge to become a successful Clinical Research Associate. Our innovative and modular training program is customized to your experience level, combining classroom learning with hands‑on experience, guided by experienced CRAs, Line Managers, and Quality Managers. Imagine yourself working for a Fortune 500 company, with world-class training and endless opportunities for growth! Many of our past trainees have gone on to exciting roles like Senior CRA, Clinical Project Manager, and Line Manager. Upon successful graduation from the training program, you will be assigned to studies as an IQVIA CRA in our Full Service model, or in our Flexible Resource model.

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: Collaborative 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 program 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 organized 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’ll be asked to complete a pre-recorded video interview and if successful after this stage we ask you to attend an assessment interview in person.
• Video interviews will take place between 15th to 23rd October 2026 . If you do not complete your video interview during this time frame, we will not be able to proceed with your application.
• Candidates successful to the assessment day in person will be notified on the week of 2nd Nov 2026.
• Interviews will be held in person in the IQVIA offices on the week of 16th November . You must be able to attend during that time frame.

Start date with IQVIA is Monday 1st February 2027.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submit