Clinical Research Associate

IQVIA; Sydney; Hybrid; AUD 70,000 - 110,000; Full time

Benefits offered by this job

Flexible hybrid work

Car and health allowances

Career growth opportunities

Job summary

IQVIA is seeking a Clinical Research Associate in Australia to monitor sites and manage trial activities in compliance with GCP/ICH guidelines. The role supports recruitment strategies, site training, and data quality across multiple Australian locations, with a flexible hybrid work setup.

The position engages with study teams, maintains regulatory documents, and ensures site performance aligns with sponsor requirements, offering visa sponsorship for eligible candidates.

Qualifications

• Bachelor's degree in science or health care.
• Minimum 9 months of independent on-site monitoring experience.
• GCP and ICH guidelines knowledge and application.
• Proficient in MS Word, Excel and PowerPoint.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH and scope of work.
• Collaborate with sites to drive subject recruitment per project needs.
• Administer protocol training and maintain regular site communication.
• Assess site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, enrollment, CRF completion, and data queries.
• Ensure TMF/ISF documents are maintained per regulatory requirements.
• Create visit reports and follow-up correspondence; liaise with study team.
• Support site start-up and overall study execution as needed.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory knowledge

Bachelor's degree in science/health

MS Office proficiency

Time management

Communication skills

Education

Bachelor's Degree in scientific discipline or health care

Tools

MS Word

MS Excel

MS PowerPoint

Laptop

iPhone

iPad

Job description

Are you aClinical Research Associatelooking for your next big adventure?

Look no further than IQVIA, a global CRO with outstanding reputation.

Our CRA teams have current openings across various locations in Australia.

*Visa sponsorship for candidates that meet the requirements and eligibility. Only suitable candidates will be contacted.

The role:

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
  

Qualifications

• Bachelor's Degree in scientific discipline or health care.
• Requires at least 9 months of independent on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Candidates will be assessed according to their years of experience and be considered for various levels where applicable.
  

What's in it for you?

• Flexible hybrid work environment, with an office in the heart of Melbourne and Sydney.
• Competitive salary with car and health allowances.
• Career growth and opportunity across our FSO and FSP models.
• Work with skilled Managers across multi-phases clinical trials
  

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 submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.