Clinical Research Job at ICON, South Korea | Life Sciences | Apply Now
If you are an early-career clinical research coordinator, an in-house study assistant, or a life sciences graduate looking to transition into a premier global Contract Research Organization (CRO), this hybrid opportunity at ICON plc is an exceptional choice. Located at our regional operations hub in Seoul, South Korea, this position places you at the intersection of international site activation, regulatory data tracking, and clinical monitoring logistics. For organized data coordinators tracking a competitive Clinical Research Job, this role (Clinical Site Associate / CSA) offers hands-on mastery over Clinical Trial Management Systems (CTMS), essential regulatory dossier collections, and site-level query resolutions. It serves as an elite corporate milestone to launch a high-trajectory ICON Career and stands out as a top-tier choice for individuals looking to secure a high-growth, hybrid Life Sciences Job within the Asia-Pacific biomedical research sector.
About The Company
ICON plc is a world-leading healthcare intelligence and global Contract Research Organization (CRO) dedicated to delivering end-to-end clinical development services. Partnering with elite global pharmaceutical, biotechnology, and medical device innovators, ICON manages multi-center clinical trials across the globe, driving the underlying medical data, regulatory submissions, and clinical logistics required to bring next-generation therapeutics to market safely. The dynamic corporate office in Seoul, South Korea, serves as a critical strategic center for East Asian clinical development. Joining the Full Service & Corporate Support clinical monitoring division as a CSA embeds you into a diverse, high-performance culture focused on nurturing early-career talent. Working under a highly flexible hybrid work model, your daily site activation tracking and documentation compliance ensure that multi-center hospital networks are optimized, fully funded, and continuously audit-ready.
Clinical Research Job – Key Responsibilities
The Clinical Site Associate functions as a vital central anchor for study teams and field monitors, taking primary operational responsibility for site readiness trackers, investigator communication networks, and administrative financial steps.
Your core site tracking, document control, and coordination duties include:
- Site Activation Governance: Supporting comprehensive site activation activities, including collecting, reviewing, formatting, and tracking essential regulatory documents and institutional approvals.
- CTMS Database Administration: Maintaining and updating real-time investigator site information, protocol statuses, and enrollment metrics within internal Clinical Trial Management Systems (CTMS) and trackers.
- CRA & Project Team Liaison: Assisting field Clinical Research Associates (CRAs) and international project leaders with routine site communications, follow-ups, and the swift resolution of site-level queries to advance this Clinical Research Job.
- Site Visit Logistics Triage: Coordinating complex logistics for investigator site visits and regional meetings, including scheduling blocks, documentation preparation, and tracking follow-up actions.
- Inspection & Audit Readiness Archiving: Ensuring accurate, chronological filing and maintenance of essential study files to guarantee uncompromised readiness for global regulatory inspections.
- Site Payment Processing Coordination: Collaborating with internal financial stakeholders and hospital research sites to support timely site payment milestone processing and invoicing issue resolutions for a premier Life Sciences Job.
- Process Improvement Contribution: Contributing directly to internal process optimization initiatives and sharing operational best practices to enhance regional site support efficiency.
Qualifications & Profile Requirements For Clinical Research Job
ICON seeks a systematic, detail-oriented team player who brings relevant scientific operations experience, strong organizational habits, and a customer-focused approach to site support.
- Required Minimum Experience Matrix:
- Industry Track Record: A minimum of one (1) year of active experience as a Clinical Site Associate (CSA), Site Management Associate (SMA), Clinical Research Associate (CRA), In-house CRA, or Global Site Initiation Team (SIT) Oncology Clinical Research Coordinator (CRC) / Study Coordinator (SC) is mandatory to anchor a successful ICON Career.
- Required Academic & Technical Criteria:
- Educational Foundation: A completed formal Bachelor’s degree in the Life Sciences or a closely related discipline (or equivalent relevant professional experience).
- Foundational working knowledge or practical initial exposure to clinical research administration, trial lifecycles, or similar highly regulated environments.
- Strong organizational and time management skills, with a proven capability to manage multiple tasks, competing priorities, and strict project deadlines.
- High attention to detail and zero-error accuracy during routine documentation review and tracking system data entry.
- Effective written and verbal communication traits, with comfort working with electronic databases and high proficiency across the standard MS Office suite.
- Ability to work collaboratively within an international team environment and adapt fluidly to changing trial priorities.
In short, the Clinical Site Associate position at ICON plc is a definitive route to translating your clinical coordination or in-house study assistant background into a premium asset within global clinical trial management. Securing an appointment here allows you to bypass general data entry roles and take direct, hybrid operational charge of the CTMS data fields, site activation dossiers, and investigator payment logistics that drive advanced clinical protocols forward. If you reside in Seoul, meet the mandatory 1-year CSA/CRC milestone baseline, and possess an analytical approach to auditing regulatory documents, apply today to secure this premier choice in a Clinical Research Job, launch an exceptional ICON Career, and lock in this outstanding Life Sciences Job.
