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(Senior) Clinical Research Associate - Job Opportunity at IQVIA

Melbourne, Australia
Full-time
Senior
Posted: March 4, 2025
On-site
AUD 120,000 - 150,000 per year based on seniority and location requirements

Benefits

World-class training and mentoring program
Exposure to diverse therapeutic areas
Global organization stability and resources
Direct sponsor interaction opportunities
Professional development pathways

Key Responsibilities

Lead site monitoring and compliance management across clinical trial lifecycle
Develop and execute strategic recruitment plans for study participants
Provide advanced site training and maintain critical stakeholder communications
Ensure protocol adherence and regulatory compliance across trial sites
Manage comprehensive study documentation and regulatory submissions
Oversee site financial operations and invoice management
Drive cross-functional collaboration for project success

Requirements

Education

Bachelor's degree in a scientific or healthcare discipline preferred

Experience

Minimum 4 years of independent on-site monitoring experience in Australia

Required Skills

GCP and ICH guidelines expertise Microsoft Office proficiency Strong written and verbal communication Organizational and problem-solving abilities Time and financial management skills Relationship building capabilities Cardiology trial management experience (preferred)

Certifications

GCP certification (implied)
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on decentralized clinical trials is reshaping monitoring approaches and requiring enhanced digital competencies Growing complexity in trial protocols is elevating the importance of experienced CRAs Rising demand for specialized therapeutic area expertise, particularly in cardiology Shift towards risk-based monitoring requiring advanced analytical skills

Role Significance

Typically part of a 5-10 person monitoring team within larger trial operations structure
Senior position with significant autonomy and responsibility for trial quality and compliance

Key Projects

Phase II-IV clinical trials in cardiology and related therapeutic areas Multi-site international studies requiring complex coordination Strategic site management and performance optimization initiatives

Success Factors

Deep understanding of clinical research regulations and ability to adapt to evolving compliance requirements Strong stakeholder management skills across multiple organizational levels Ability to balance quality requirements with operational efficiency Proactive problem-solving approach to site management

Market Demand

High demand with significant growth projected due to increased clinical trial activity in Australia and APAC region

Important Skills

Critical Skills

Independent monitoring experience is essential due to role autonomy and responsibility Therapeutic area expertise, particularly in cardiology, for specialized trial management Regulatory knowledge for ensuring compliance and quality standards

Beneficial Skills

Project management capabilities for career advancement Digital health technology familiarity for evolving trial landscapes Business acumen for site budget management

Unique Aspects

Sponsor-dedicated role offering deep therapeutic area specialization
Combination of CRO stability with sponsor-side exposure
Strong focus on cardiology trials indicating strategic therapeutic area focus
Comprehensive training program suggesting investment in long-term talent development

Career Growth

2-4 years in role before progression, depending on performance and organizational growth

Potential Next Roles

Clinical Research Manager Project Manager Clinical Operations Director Regional Monitoring Manager

Company Overview

IQVIA

IQVIA is a global leader in clinical research and healthcare intelligence, formed from the merger of IMS Health and Quintiles

Top-tier CRO with significant market share and extensive global presence
Strong APAC footprint with established operations in major Australian cities
Professional corporate environment with emphasis on quality and compliance, balanced with innovation and personal development
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