Clinical Research Associate, FSP

🔥 12 minutes ago

🇰🇷 South Korea – Remote

⏰ Full Time

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 15%

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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 the current approved protocol and protocol amendments, ICH GCP, 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 • Thrive in multi-national project teams and deliver exemplary customer service across multiple projects • Perform and coordinate all aspects of the clinical monitoring process • Conduct monitoring activities independently

🎯 Requirements

• University degree in a nursing / life-sciences field • Experience of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation (at least for 3 years) • Demonstrated understanding of ICH-GCP, MFDS and FDA requirements • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology • Exceptional communication, collaboration, organizational and time management skill • Fluency in English languages • Ability to conduct monitoring activities independently

🏖️ Benefits

• Sign-on bonus • Award winning training programmes that will assist your technical and professional skills and knowledge

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