FSP CRA

🔥 32 minutes ago

🇰🇷 South Korea – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Ensure clinical studies are conducted at investigator sites in compliance with approved protocols and amendments, ICH GCP, client/PPD written standards, and applicable local laws and regulatory requirements • Protect the rights, safety and well-being of human subjects • Ensure reported study data is accurate, complete and verifiable from source documents • Perform and coordinate all aspects of the clinical monitoring process • Conduct monitoring activities independently • Work within multinational project teams • Deliver exemplary customer service across multiple projects • Take ownership of assigned work

🎯 Requirements

• University degree in a nursing / life-sciences field • At least 2 years of independent, on-site monitoring experience in a pharmaceutical company or clinical research organisation • Understanding of ICH-GCP, MFDS and FDA requirements • Understanding of medical/therapeutic area knowledge and medical terminology • Exceptional communication, collaboration, organizational and time management skills • Fluency in English

🏖️ Benefits

• Sign-on bonus • Award-winning training programmes • Technical and professional skills development

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