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1+ years stated
University degree in nursing or life sciences
fixed
Standard Mon-Fri
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What this posting tells you
Senior Clinical Research Associate role with GSK sponsor. Fully remote position based in South Korea with standard Monday to Friday schedule. Requires at least 1 year independent on-site monitoring experience in pharmaceutical or clinical research organization, university degree in nursing or life sciences, and knowledge of ICH-GCP, MFDS, FDA requirements. Benefits include sign-on bonus and professional training programs.
Customer success, Data, DevOps, Education, Healthcare admin, Operations, Product, Security, Customer support
Korea, Republic of
Asia/Seoul
Mid-level · full_time
- Compensation is not listed
Customer success hiring on WFH.team
Category counts come from WFH.team's latest published remote job market snapshot.
Explore the remote job marketFSP CRA (Sponsor: GSK) ─ with Sign-on Bonus at 110181-0039301 PPD Development (S) Pte. Ltd. Korea Branch
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
CRA (Sponsor: GSK) ─ with Sign-on Bonus
What you’ll do
This individual ensures that clinical studies are conducted at investigator sites in compliance with:
- the current approved protocol and any protocol amendment(s),
- ICH GCP
- GSK/PPD Written Standards
- applicable local laws and regulatory requirement(s)
so that the rights, safety and well-being of human subjects is protected and that the reported study data is accurate, complete, and verifiable from source documents.
Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, exciting projects.
Have excellent communication and social skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
Perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.
Benefit from award winning training programmes that will assist your technical and professional skills and knowledge.
Keys to Success
- Education - University degree in a nursing / life-sciences field
- Experience - Experience of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation ( at least for 1 year )
- Knowledge, Skills, Abilities- 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