Clinical Research Associate

Pharmaceutical Research Associates, Inc; Council of the City of Sydney; Remote; AUD 80,000 - 100,000; Full time

Job summary

A global clinical research organization is seeking a Senior Clinical Research Associate to support Oncology studies. This home-based role in Australia involves responsibilities such as site management, mentoring team members, and ensuring data quality. Candidates should have a degree in Pharmacy and at least 2 years of monitoring experience. A competitive salary and various benefits are offered.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum 2+ years prior monitoring experience with global trials.
• Ability to mentor other team members.

Responsibilities

• Perform all aspects of CRA duties from site selection to database lock.
• Ensure high quality data resulting in low query levels.
• Support and mentor team members.

Skills

Oncology monitoring experience

Excellent communication skills

International guidelines ICH-GCP knowledge

Education

Degree in Pharmacy or related course

Job description

Overview

(Senior) Clinical Research Associate FSP Global Pharma

Location: home-based in Sydney, Brisbane or Melbourne

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

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives. You will be embedded in our client's Oncology study team and have a dedicated ICON line manager to support you.

Responsibilities

What you will be doing:

• Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
• You will be embedded in our client's study team and have a dedicated ICON line manager to support you
• Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports
• Support and mentor other team members

Qualifications

You are:

• Degree in Pharmacy or any related course
• Min.2+ years prior monitoring experience with global trials
• Strong Onoclogy monitoring experience
• Excellent communication skills
• Excellent knowledge of international guidelines ICH-GCP, good knowledge of local regulations
• Flexibility to travel and to work from the sponsor office occasionally (if in Sydney and if not traveling)

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 maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt 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, 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 through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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