
10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
🔥 0 minutes ago
🗣️🇰🇷 Korean Required
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10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
• Perform study activities including start-up, maintenance, and close-out with Clinical Operations team members’ oversight and guidance • Perform eTMF functional QC and CRO oversight QC for PMS • Upload study documents to the Trial Master File or other repositories • Review and participate in quality assurance of data or documents • Assist with development of documents and standard forms • Arrange study meeting logistics and agendas, and assist with minutes • Track and prepare study-specific information using databases, spreadsheets, and other tools • Maintain internal Clinical Operations databases, tools, and document repositories • Provide administrative support for study-related activities under Clinical Operations supervision • Act as a local subject matter expert or single point of contact for a specific focus area when needed • Interact with other departments to complete assigned tasks • Ensure work complies with established practices, policies, processes, and regulatory requirements
• Minimum 1 or more years’ relevant work experience in SSU, CTA, or as a Study Coordinator from investigational sites in Pharma/CRO • BA / BS / RN • Knowledge of local country regulations, ICH Guidelines, GCP, and standard clinical operating procedures • eTMF, CTMS, and SSU(A) experience preferred • Basic office programs/tools proficiency • Excellent verbal and written Korean and English skills • Clear and concise communication skills • Ability to support a team-oriented, highly matrixed environment • Ability to execute multiple assigned tasks • Ability to work proactively under minimal supervision • Ability to be a fast learner • Flexibility and adaptability to change
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Collaborate with passionate problem solvers • Specialized therapeutically or functionally aligned teams • Diverse team of experts • Career paths and employment opportunities
Apply Now🕒 6 days ago
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