Clinical Research Associate

Role overview

IQVIA is hiring Clinical Research Associates for opportunities across several locations in Australia. This role focuses on site monitoring and study oversight to help ensure clinical trials are run according to the protocol, relevant regulations, and sponsor expectations.

What you will do

• Carry out site visits covering selection, initiation, routine monitoring, and close-out, following the agreed scope of work and all applicable GCP and ICH requirements.
• Partner with study sites to shape, manage, and follow recruitment plans so enrolment stays aligned with project goals.
• Deliver protocol and study-specific training to assigned sites and keep communication channels active to address ongoing needs and issues.
• Review the quality and completeness of site conduct and escalate any compliance or quality concerns when necessary.
• Track study progress by monitoring ethics/regulatory submissions, approvals, recruitment, enrolment, CRF completion, query resolution, and related milestones; support study start-up where needed.
• Make sure site records are complete and filed correctly in the TMF, and confirm the ISF is maintained in line with GCP and local regulatory standards.
• Prepare ongoing site management records, including monitoring notes, visit reports, follow-up letters, and other required documentation.
• Work closely with internal study team members to support smooth project execution.
• Where relevant, contribute to site-level recruitment planning.
• Where relevant, help manage site finances in line with the clinical trial agreement and local invoicing requirements.

What the role requires

• A bachelor’s degree in a scientific or healthcare-related discipline.
• At least 9 months of independent on-site monitoring experience.
• An equivalent mix of education, training, and experience may be accepted in place of a degree.
• Working knowledge of clinical research regulations, especially GCP and ICH guidelines, and the ability to apply them in practice.
• Sound understanding of therapeutic areas and study protocols, based on company training.
• Strong computer literacy, including Microsoft Word, Excel, and PowerPoint, plus comfort using a laptop, iPhone, and iPad where relevant.
• Good organization, problem-solving, time management, and financial management skills.
• Ability to build productive working relationships with colleagues, managers, and clients.
• Candidates may be considered for different levels based on experience.

What IQVIA offers

• A flexible hybrid working setup, with offices located in central Melbourne and Sydney.
• A competitive salary package that includes car and health allowances.
• Opportunities for career progression across FSO and FSP models.
• The chance to work alongside experienced managers on multi-phase clinical trials.

Additional information

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare sectors. The company focuses on building intelligent connections that support the development and commercialization of innovative treatments and better health outcomes worldwide.

Hiring integrity notice

IQVIA maintains a zero-tolerance approach to fraud in the recruitment process. All information provided in an application must be accurate and complete. Any false, misleading, or omitted information may lead to immediate rejection or later termination of employment, subject to applicable law.