CTA Job Opportunity at IQVIA | Apply Now
Looking for a CTA job in Australia? IQVIA is currently hiring a Clinical Trials Assistant 1 (1 Year Contract, Sponsor Dedicated) in Melbourne, Australia. This exciting opportunity allows candidates with clinical research experience to support clinical trial operations, manage study documentation, and work alongside experienced clinical research professionals. If you are seeking IQVIA careers and a rewarding job in Australia, this position could be the ideal next step in your clinical research career.
- Job Position: Clinical Trials Assistant 1 (CTA)
- Company: IQVIA
- Location: Melbourne, Australia
- Job ID: R1547174
About the Company
IQVIA careers provide opportunities to work with one of the world’s leading healthcare and clinical research organizations. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections to accelerate the development and commercialization of innovative medical treatments that help improve patient outcomes and population health worldwide.
CTA Job Description
CTA job opportunities at IQVIA involve supporting clinical research projects through administrative and operational activities. IQVIA is currently seeking a Clinical Trials Assistant (CTA) to join its Functional Service Partnerships team in a client-facing role. As a vital part of the team, CTAs perform daily administrative tasks to support clinical projects and update clinical systems and databases. Applicants must have full unrestricted Australian work rights. Contract renewal or conversion is dependent on business needs.
The successful candidate will perform general administrative tasks as needed and demonstrate excellent communication, computer, and problem-solving skills. Candidates should be resourceful, analytical, adaptable, organized, and capable of building rapport with peers and site staff.
Qualifications
CTA job applicants should possess relevant clinical research experience and strong administrative capabilities.
- Minimum 6–12 months experience in a CTA role.
- Flexible and adaptable to different levels of education, training, and experience.
- Updated and maintained clinical documents and systems accurately (e.g., eTMF and CTMS).
- Communicated effectively with clients and stakeholders.
- Mastered various computer applications and resolved complex issues.
- Familiar with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Ensured compliance in all clinical trials.
- Completed High or Secondary School diploma/certificate.
Required Skills
IQVIA careers value candidates with strong clinical research and administrative skills.
- Clinical trial administration
- Documentation and data management
- eTMF and CTMS proficiency
- Communication and stakeholder management
- Problem-solving and organizational skills
- Attention to detail
- Knowledge of GCP, ICH, and regulatory compliance
- Clinical systems management
CTA Job – Key Responsibilities
CTA job responsibilities include supporting clinical trial documentation, systems, and project administration activities.
- Prepare, handle, distribute, file, and archive clinical documentation and reports as per the scope of work and standard operating procedures.
- Review study files periodically for completeness and accuracy.
- Support CRAs and RSU with the management of Clinical Trial Supplies and tracking information.
- Track and manage CRFs, queries, and clinical data flow efficiently and effectively.
- Communicate with the clinical team and provide relevant project information, correspondence, and documentation.
- Perform general administrative tasks as required.
- Update clinical systems and databases accurately.
- Maintain organized study records and documentation.
Why Join IQVIA?
Job in Australia opportunities at IQVIA offer exposure to global clinical research projects and industry-leading expertise.
- Work with a globally recognized clinical research organization.
- Gain valuable experience in sponsor-dedicated clinical trials.
- Collaborate with experienced clinical research professionals.
- Develop expertise in clinical trial operations and documentation.
- Hybrid working environment.
- Opportunity for future contract renewal or conversion based on business requirements.
