CRA I

Pharmaceutical Research Associates, Inc; Gauteng; On-site; ZAR 400,000 - 600,000; Full time

Job summary

A leading clinical research organization seeks a Clinical Research Associate (CRA) to ensure patient safety and data integrity in clinical trials. The successful candidate will monitor trial compliance, verify participant protections, and report findings. Candidates should hold a relevant degree and have experience in clinical trials.

Benefits

Competitive salary

Diverse culture

Work-life balance opportunities

Qualifications

• Previous experience in clinical trials required, including 1 year on-site monitoring.
• Experience in oncology is a plus.
• Fluency in English and host language is needed.

Responsibilities

• Completes onsite and remote monitoring activities according to ICH-GCP guidelines.
• Ensures participant protection by confirming informed consent and protocol compliance.
• Writes and submits reports of investigational site findings.

Skills

Monitoring clinical trials

Patient safety

Data integrity

Education

Bachelor’s degree in health or life sciences

Job description

Overview

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, 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.

Responsibilities

What you will be doing:

A CRA is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.

• 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 1 year of on-site monitoring experience.
• 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.