Tenant Insights Research Associate

Hatch; North Sydney; On-site; AUD 60,000 - 90,000; Full time

Job summary

IQVIA is recruiting for a Clinical Research Associate Trainee Program in Sydney. The role involves participating in a full-time training program that covers all aspects of clinical trial monitoring, with supervision on site visits and regulatory activities.

The program includes mentorship and learning clinics to develop practical competencies. Successful candidates will have a health-care or life-science degree, strong English communication, and a proactive, detail-oriented mindset.

Qualifications

• Bachelor's degree in health care or life-science field or equivalent experience.
• Prior experience in a clinical research setting is advantageous.
• Basic understanding of ICH-GCP and Australian regulatory requirements.
• 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, dedicated CRA trainee program covering all aspects of clinical trial monitoring.
• Learn and apply ICH-GCP guidelines and Australian ethical and regulatory requirements.
• Conduct site monitoring visits under supervision, including initiation, monitoring, and close-out.
• Assist in managing study progress by tracking regulatory submissions, recruitment and data completion.
• Maintain accurate study documentation (TMF and ISF) and collaborate with study teams.

Skills

Communication

Time management

Critical thinking

MS Office

Education

Bachelor's degree in health care or life-science

Tools

MS Office Suite

Job description

Clinical Research Associate Trainee Program (Sydney)

North Sydney, New South Wales, Australia
Full time

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.

Our Cutting‑Edge Training Program:

• 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.

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