Clinical Research Associate – Sponsor, Biogen

🔥 0 minutes ago

🇰🇷 South Korea – Remote

⏰ Full Time

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 the current approved protocol and 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 • At least 3 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

🏖️ Benefits

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