CRA II

Pharmaceutical Research Associates, Inc; Gauteng; On-site; ZAR 600,000 - 900,000; Full time

Job summary

A leading clinical research organization seeks a Clinical Research Associate to handle monitoring activities across clinical trials. You will ensure compliance, protect participant integrity, and contribute to innovative health solutions amidst a dynamic team. This role offers a chance to support groundbreaking medical developments that address critical health challenges across the globe.

Benefits

Diverse culture and environment

Competitive salary

Work-life balance opportunities

Qualifications

• Experience in supporting clinical trials, especially in oncology is a plus.
• Minimum of 4 years on site monitoring tasks.
• Ability to write reports and submit findings.

Responsibilities

• Completes onsite and remote monitoring activities.
• Verifies informed consent procedures.
• Ensures data integrity and compliance with protocols.
• Prepares for audits and provides training.

Skills

Fluent English

Monitoring clinical trials

Protocol compliance

Data integrity assurance

Education

Bachelor’s degree in a health, life sciences or relevant field

Job description

Overview

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

You will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s and infectious diseases. Be ready to work in a solid partnership and an environment driven by innovation and continuous improvement.

Responsibilities

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes.
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Participates in audit preparation and follow-up activities as needed.
• May serve as preceptor, providing training to less experienced clinical team members.

Qualifications

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study.
• Previous experience supporting clinical trials including 4 years of experience on site monitoring tasks.
• Previous experience in oncology is a plus.
• Travel is required.
• All employees must read, write and speak fluent English and host country language.

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.

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.