Clinical Research Associate II/ Senior Clinical Research Associate

ICON; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

ICON is seeking a Clinical Research Associate II/Senior Clinical Research Associate for a home-based role in the United States. This position involves managing clinical trials, ensuring data quality, and supporting study teams. The ideal candidate will have a degree in Pharmacy and relevant monitoring experience, particularly in Oncology. ICON values diversity and offers competitive benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance options

Competitive retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• 2+ years of prior monitoring experience with global trials.
• Oncology monitoring experience is desirable.

Responsibilities

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

Skills

Communication

Knowledge of international guidelines (ICH-GCP)

Education

Degree in Pharmacy or related field

Job description

Title: Clinical Research Associate II / Senior Clinical Research Associate

Location: Melbourne, Sydney (home-based)

As an experienced Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

You will be part of an innovative and global biotechnology company, which prides itself on being one of the world's leading independent biotechnology companies. They focus on areas with unmet medical needs, with the ambition to help reduce the social and economic burden of disease in society today. In this role, you will have the opportunity to work on cutting-edge early development trials, including Oncology/Hematology, as well as a broad range of other therapeutic areas.

What you will be doing:

1. Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits, close-out visits, and database lock.
2. Be embedded in our client's study team with a dedicated ICON line manager for support.
3. Oversee all aspects of study site management to ensure high-quality data, resulting in low query levels and good Quality Assurance reports.

You are:

• Degree in Pharmacy or related field.
• 2+ years of prior monitoring experience with global trials.
• Oncology monitoring experience is desirable.
• Excellent communication skills.
• Strong knowledge of international guidelines (ICH-GCP) and good knowledge of local regulations.
• Flexibility to travel.

What ICON can offer you:

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements.
• A range of health insurance options for you and your family.
• Competitive retirement planning options.
• Global Employee Assistance Programme, TELUS Health, offering 24/7 support.
• Life assurance.
• Flexible country-specific benefits like childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments.

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

At ICON, inclusion & belonging are fundamental. We are committed to providing an inclusive environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, religion, gender, or disability. If you need accommodations during the application process, please let us know at https://careers.iconplc.com/reasonable-accommodations.

We encourage you to apply even if you do not meet all requirements—you might be exactly what we’re looking for.

#LI-KA1

#LI-Remote