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CRA - FSP - Job Opportunity at Parexel

Canberra, Australia
Full-time
Mid-level
Posted: March 19, 2025
Hybrid
AUD 85,000 - 110,000 per year based on Canberra market rates and industry standards

Benefits

Structured professional development pathway
Industry-standard healthcare benefits inferred
Flexible work arrangements with remote options
Global mobility opportunities

Key Responsibilities

Lead site relationship management and protocol compliance oversight for clinical trials
Ensure data integrity and regulatory compliance across multiple research sites
Drive site performance optimization and issue resolution
Manage end-to-end clinical trial documentation and systems
Coordinate cross-functional stakeholder communication

Requirements

Education

Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience

Experience

Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology

Required Skills

Sound problem solving skills Able to take initiative and work independently Advance presentation skills Client focused approach to work Ability to interact professionally within a client organization Flexible attitude with respect to work assignments and new learning Ability to prioritize multiple tasks and achieve project timelines Strong computer skills including CTMS, EDMS, and MS-Office Strong interpersonal, verbal, and written communication skills Effective time management Consulting Skills Great attention to detail
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Sauge AI Market Intelligence

Industry Trends

The clinical research industry is experiencing rapid digitalization with increased adoption of decentralized trial methodologies and remote monitoring capabilities Growing emphasis on real-world evidence and adaptive trial designs is reshaping CRA responsibilities Rising demand for CRAs who can navigate complex data management systems and ensure compliance with evolving regulatory frameworks

Role Significance

Typically works within a study team of 5-8 members, including other CRAs, data managers, and project managers
Mid-level position with significant autonomy in site management and protocol oversight responsibilities

Key Projects

Phase II-IV clinical trials management Site performance optimization initiatives Regulatory compliance and audit preparation programs Site staff training and development

Success Factors

Strong grasp of GCP guidelines and regulatory requirements Excellent stakeholder management and communication abilities Proven ability to maintain data integrity while managing multiple competing priorities Adaptability to evolving clinical research technologies and methodologies

Market Demand

High demand with steady growth projected due to expanding clinical trial activity in Asia-Pacific region and increasing complexity of trial protocols

Important Skills

Critical Skills

GCP and regulatory compliance expertise Site relationship management Clinical data verification and quality oversight Problem-solving and issue escalation judgment

Beneficial Skills

Experience with decentralized trial methodologies Understanding of risk-based monitoring approaches Knowledge of emerging clinical research technologies Therapeutic area specialization

Unique Aspects

FSP (Functional Service Provider) model indicates dedicated client alignment with potential for deep therapeutic area expertise development
Strong focus on technology integration and remote monitoring capabilities
Emphasis on cross-cultural competency for global trial management

Career Growth

2-3 years in role before advancement, depending on performance and project complexity exposure

Potential Next Roles

Senior CRA Clinical Project Manager Clinical Operations Manager Regional Monitoring Manager

Company Overview

Parexel

Parexel is a leading global CRO with extensive experience in managing complex clinical trials across multiple therapeutic areas

Top-tier CRO with strong presence in APAC region and global markets
Strategic position in Canberra supports growing clinical trial activity in Australia and broader APAC region
Matrix organization emphasizing collaboration, professional development, and work-life balance
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