Senior Project Specialist

Syneos Health

Sr. Project Specialist supporting clinical trial start-up, maintenance, and close-out for Syneos Health’s life sciences services.

Posted 8/11/2026full-timeRemote • 🇰🇷 South KoreaSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Operations, including eTMF management, regulatory compliance, and quality assurance processes. Proficient in coordinating study activities and maintaining documentation in a fast-paced, team-oriented environment.

Highest-signal resume keywords

Clinical Operations ExperienceETMF ManagementKnowledge of ICH GuidelinesExcellent Korean and English Communication SkillsRegulatory Compliance

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Study CoordinationQuality AssuranceDocument ManagementData TrackingRegulatory Requirements Knowledge

Soft Skills

Clear CommunicationTeam CollaborationProactive Problem SolvingFlexibilityAdaptability

Tools & Technologies

ETMFCTMSDatabasesSpreadsheetsOffice Programs

Certifications & Qualifications

BABSRN

Industry Keywords

PharmaCROSSUCTAGCP

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

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