Clinical Research Associate - Oncology

Worldwide Clinical Trials is seeking a Clinical Research Associate specializing in Oncology to join their team in Seoul, South Korea. This role is crucial for advancing clinical research and improving patient lives by working with brilliant minds across diverse therapeutic areas. Join a global, midsize CRO that pushes boundaries and innovates to find cures for persistent diseases.

As a Clinical Research Associate (CRA), you will be instrumental in conducting site qualification, initiation, monitoring, and close-out visits. You will collaborate with a supportive and team-oriented environment, contributing to a mission of working with passion and purpose every day to improve lives. If you are looking for a role where your contributions make a profound impact, apply now!

Company Overview

Worldwide Clinical Trials is a global CRO serving development-driven biopharmaceutical companies, with over 4,400 professionals operating across more than 70 countries. They deliver therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, supporting every development phase. Their flexible service model, powered by a people-first, partnership-driven approach, strengthens collaboration and supports tailored solutions.

They are a global, midsize CRO that pushes boundaries and innovates, built by those who take pioneering, creative approaches. With a mission to work with passion and purpose every day to improve lives, Worldwide Clinical Trials fosters a diverse and inclusive environment where professionals from all backgrounds can succeed and thrive.

Quick Details

• Salary Range: Not Specified
• Job Type: Full-time
• Qualifications: Bachelors Degree or RN/BSN in Nursing
• Experience: 2+ years of experience as a Clinical Research Associate

Key Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.

Requirements

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS and EDC Systems.
• Experience in Oncology is required.
• Willingness to travel required.

Benefits

• Work in a global, midsize CRO that pushes boundaries and innovates.
• Be part of a team that works with passion and purpose every day to improve lives.
• Contribute to finding cures for the world's most persistent diseases.
• Join a diverse and inclusive environment where professionals from all backgrounds can succeed.
• Receive extensive support through regulatory submissions, TMF management, and in-house CRAs.