FSP CRA

🕒 September 14

🇰🇷 South Korea – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 18%

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

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Ensure clinical studies are conducted at investigator sites in compliance with approved protocols, ICH GCP, Client/PPD Written Standards, and applicable laws and regulations • 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 in multinational project teams • Deliver exemplary customer service across multiple projects • Take ownership of clinical research work in a collegiate environment

🎯 Requirements

• University degree in a nursing / life-sciences field • At least 2 years of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation • 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 • Compliance with current approved protocols and amendments, ICH GCP, Client/PPD Written Standards, applicable local laws and regulatory requirements

🏖️ Benefits

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

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