ICON: Clinical Research Associate – Life Sciences/Health Sciences Graduates Apply Now
ICON is an innovative and global Biotechnology company, recognized as one of the world’s leading independent biotechnology firms. Our focus is on areas with unmet medical needs, aiming to reduce the social and economic burden of disease in today’s society.
About the Role:
As a Clinical Research Associate (CRA) at ICON, you will be part of the world’s largest and most comprehensive clinical research organization, driven by healthcare intelligence.
Job Responsibilities:
- Completing onsite and remote monitoring activities in accordance with ICH-GCP guidelines, regulations, SOPs, and study processes.
- Verifying the protection of study participants by ensuring adherence to informed consent procedures.
- Ensuring the integrity of clinical data and compliance with approved protocol, GCP, regulations, and SOPs.
- Writing reports of investigational site findings and participating in audit preparation activities.
- Providing training to less experienced clinical team members and handling clinical tasks as needed.
Requirements:
To excel in this role, you should have:
- Bachelor’s degree in a health, life sciences, or related field.
- Previous experience supporting clinical trials with on-site monitoring experience.
- Experience in oncology is an advantage.
- Willingness to travel as needed.
- Fluency in English and host country language.
What ICON Offers:
At ICON, we value our people and strive for a diverse, high-performance culture. In addition to competitive salaries, we offer a range of benefits to support your well-being and work-life balance.
Learn more about the benefits of working at ICON on our careers website.
Join our team at ICON and be part of cutting-edge clinical research in Chile. Apply now!
Keywords: Clinical Research Associate, CRA, Healthcare, Clinical Trials, ICH-GCP, Oncology, Biotechnology, ICON
