Remote Investor Materials Evaluator For Fundraising

Mercor; Sydney; Remote; AUD 80,000 - 120,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

LifeWorks EAP program

Life assurance

Job summary

ICON Strategic Solutions is seeking a CRA II in Melbourne with remote work options. You will design and monitor clinical trials, review data, and ensure protocol compliance and patient safety.

The role requires strong collaboration with investigators and site staff across multiple sites.

Qualifications

• Bachelor’s degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Knowledge of clinical trial processes and ICH-GCP guidelines.
• Strong organizational and communication skills; attention to detail.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance and patient safety throughout trials.
• Collaborate with investigators and site staff to facilitate study conduct.
• Perform data review and resolve queries to ensure high-quality data.
• Assist in preparation and review of study documentation.

Skills

Clinical research

Site monitoring

Data integrity

Regulatory knowledge

Travel flexibility

Education

Bachelor's degree in scientific/healthcare

Tools

ICH-GCP guidelines

Job description

CRA II - Melbourne, Australia Remote

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:

• 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:

• 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:

• 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, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated 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, color, 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 or submit a request here. If you are a current ICON Employee, you can apply directly through our internal portal.