Clinical Research Associate - Trainee Program at IQVIA. - Turkey

Auckland, Auckland, New Zealand -

Full Time

Start Date

Immediate

Expiry Date

23 Dec, 25

Salary

0.0

Posted On

24 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Critical Thinking, Detail-Oriented, Proactive, Communication Skills, Problem-Solving, Time Management, Team Collaboration, Understanding of ICH-GCP, MS Office Proficiency

Industry

Hospitals and Health Care

Description

Assoc CRA Trainee Program Auckland New Zealand - now taking applications for our next intake commencing on the 12th January 2026 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 Training Program in Auckland New Zealand. Applications close Friday 3rd October. 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. We focus on "Train," "Transfer," and "Sustain" – ensuring you master the concepts, gain on-the-job competence, and receive continuous evaluation and support. At IQVIA, we are always learning. 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, online testing and if successful after this stage we ask you to attend an assessment interview in person Video interviews and online assessment will take place between 25th September to the 15th October. Candidates successful to the assessment day in office will be notified by 23rd October 2025. Applications close Friday 3rd October 3pm Interviews for New Zealand will be held at our Office on Thursday 30th October. This dates is fixed. Start date with IQVIA is Monday 12th January 2026 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 a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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Responsibilities

Participate in a full-time training program covering all aspects of clinical trial monitoring. Conduct site monitoring visits under supervision and assist in managing study progress.