Senior CRA/ CRA II

ICON Strategic Solutions; Sydney; A distancia; AUD 80.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning offerings

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Descripción de la vacante

A leading clinical research organization is seeking a Clinical Research Associate II in Sydney. This role involves overseeing clinical trial duties and managing study sites to ensure high-quality data. The ideal candidate has a degree in Pharmacy, with at least 2 years of relevant experience and excellent communication skills. The company offers competitive benefits and is committed to a diverse, inclusive workplace.

Formación

• 2+ years of on-site monitoring experience within CRO/Pharma/Biotech.
• Excellent knowledge of ICH-GCP guidelines and good knowledge of local regulations.

Responsabilidades

• Perform all aspects of CRA duties from site selection to database lock.
• Oversee all aspects of study site management to ensure high-quality data.

Conocimientos

On-site monitoring experience

Excellent communication skills

Adaptability to a dynamic environment

Knowledge of ICH-GCP guidelines

Flexibility to travel

Educación

Degree in Pharmacy or a related field

Descripción del empleo

Overview

Role: Clinical Research Associate II / Senior Clinical Research Associate FSP

Location: Melbourne / Sydney / Brisbane / Adelaide (home-based)

As an experienced Clinical Research Associate, you will be joining the world’s largest and most comprehensive clinical research organisation, powered by healthcare intelligence. You will partner with one of the world’s premier Biopharmaceutical companies, working across a broad portfolio of medicines and vaccines with a long history of delivering innovative treatments and preventive medicines globally.

What You Will Be Doing

• Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits, close-out visits, and database lock.
• Be fully embedded in the client’s study team with a dedicated ICON line manager to support you.
• Oversee all aspects of study site management to ensure high-quality data resulting in consistently low query levels and strong Quality Assurance reports.

You Are

• Degree in Pharmacy or a related field
• 2+ years of on-site monitoring experience within CRO/Pharma/Biotech
• Excellent communication skills
• Adaptability to work in a dynamic environment
• Excellent knowledge of ICH-GCP guidelines and good knowledge of local regulations
• Flexibility to travel

What ICON Can Offer You

Our success depends on the quality of our people. ICON is committed to a diverse, high-performance culture that rewards talent and nurtures growth. In addition to a competitive salary, ICON offers a range of benefits designed to support wellbeing and work-life balance for you and your family.

• Various annual leave entitlements
• Health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings
• Global Employee Assistance Programme (24/7 access to a global network of professionals)
• Life assurance
• Flexible country-specific optional benefits (e.g., childcare vouchers, gym discounts, travel passes, health assessments, etc.)

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

ICON is committed to inclusion and belonging. We provide an inclusive and accessible environment for all candidates and equal opportunity in employment. If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role but unsure if you meet all requirements? We encourage you to apply anyway — there’s every chance you’re exactly what we’re looking for at ICON.