Remote Admin Va For Research Studies | Flexible, Part-Time

Afg Inc; Sydney; Hybrid; AUD 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Health insurance

Annual leave

Retirement planning

Employee assistance program

Life assurance

Childcare vouchers

Travel benefits

Zusammenfassung

ICON Strategic Solutions is hiring a CRA II in Sydney, Australia. You will design and analyze clinical trials, interpret complex data, and contribute to patients' treatment advances.

Responsibilities include site visits, data integrity, and collaboration with investigators. Requires a science/healthcare degree, 2+ years CRA experience, and willingness to travel ~60%.

Qualifikationen

• Bachelor's degree in a scientific or healthcare-related field is required.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Aufgaben

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity and patient safety.
• Collaborate with investigators and site staff for smooth study conduct.
• Perform data review and resolve queries to maintain data quality.
• Prepare and review study documentation such as protocols and reports.

Kenntnisse

Clinical trial monitoring

ICH-GCP

Communication skills

Organizational skills

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Jobbeschreibung

CRA II Sydney Australia
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

**What You Will Do:**

Key responsibilities include:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

**What ICON can offer you:**

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well‑being.
• Life assurance
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position, please let us know.