Clinical Research Associate 2 at IQVIA

Melbourne, Victoria, Australia

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Pharmaceuticals, HealthcareIndustries

Requirements

Bachelor’s in science or healthcare (or equivalent experience)
2+ years of on-site monitoring experience
Experience in Haematology and Oncology
Strong grasp of GCP/ICH and clinical trial protocols
Tech-savvy: MS Office, iPhone/iPad, and remote tools
Excellent communication, organization, and problem-solving skills
Ability to build strong relationships with sites and teams
Minimum of 18 months monitoring experience (Perth or Brisbane based)

Responsibilities

Lead site visits (selection, initiation, monitoring, close-out) per GCP/ICH standards
Drive subject recruitment and site engagement to meet study goals
Deliver protocol training and maintain strong site communication
Monitor site performance, escalate quality issues, and ensure regulatory compliance
Track study progress: submissions, enrollment, CRFs, and data queries
Maintain Trial Master File (TMF) and Investigator Site File (ISF)
Document findings and follow-ups with clear, timely reports
Collaborate with cross-functional teams to support project execution
Manage site budgets and invoicing (if applicable)

Skills

GCP/ICH

Clinical Monitoring

Site Management

TMF

ISF

Protocol Training

Regulatory Compliance

MS Office

Haematology

Oncology

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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