Project Manager

Worldwide Clinical Trials

. Manage one or more allocated Phase I through IV clinical trials, which may be local, regional, or global in scope .

Posted 10/27/2026full-timeRemote • South KoreaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in managing Phase I through IV clinical trials, ensuring compliance with ICH Guidelines and GCP, while effectively leading project teams and maintaining strong client relationships. Proficient in project management processes, with a focus on delivering projects on time and within budget in a multi-office environment.

Highest-signal resume keywords

Clinical Project ManagementICH Guidelines KnowledgeGCP ComplianceClient Relationship ManagementTeam Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Management ProcessesClinical Trial CoordinationData InterpretationContingency PlanningFinancial Performance ManagementDrug Development Process KnowledgeRegulatory Requirements UnderstandingTraining and Development Needs AssessmentPerformance Appraisal ContributionMulti-Office Project Management

Soft Skills

Excellent CommunicationOrganizational SkillsInterpersonal SkillsProblem-Solving SkillsTeamwork Promotion

Tools & Technologies

SOPsClinical Trial Management Systems

Certifications & Qualifications

University/College Degree in Life Science or Related FieldCertification in Allied Health Profession

Industry Keywords

Clinical TrialsPharmaceutical IndustryCRORegulatory ComplianceHealth Care Setting

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage one or more allocated Phase I through IV clinical trials, which may be local, regional, or global in scope
Coordinate and manage clinical trials from start-up through close-out activities
Direct the technical, financial, and operational aspects of projects
Work with functional area leads to identify and evaluate project requirements, interpret complex data, and implement contingency or rescue strategies
Ensure project deliverables meet customer time, quality, cost, and contract expectations
Lead core project team members and facilitate leadership of extended or complete project teams
Lead internal and external cross-unit coordination, including subcontractors
Define and manage project resource needs and establish contingency plans
Design, implement, track, and revise project plans
Promote teamwork and resolve conflicts
Communicate project-related matters with Project Management leadership
Meet financial performance targets for assigned clinical projects
Initiate improvements to enhance work efficiency and quality
Act as key client contact and maintain strong client relationships
Ensure project staff are trained on protocols and study processes and comply with professional standards, SOPs, GCP, and local regulations
Identify training and development needs and contribute to performance appraisals
Manage delegated aspects of designated projects
Perform other duties assigned by management

Requirements

What you’ll need

University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution, or equivalent combination of education and experience
Minimum of five (5) years of clinical pharmaceutical industry experience, including demonstrated skills and competency in clinical project management tasks
Alternatively, more than five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries, or proven relevant clinical development experience and skills
Thorough knowledge of project management processes
Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements for clinical development programs
Available for domestic and international travel, including overnight stays
Valid current passport required
Ability to drive and have a valid driver’s license
Fluent in local office language and English, written and verbal
Broad knowledge of the drug development process and client needs
Demonstrated ability to manage projects in a multi-office environment
Ability to handle multiple competing priorities and utilize resources effectively
Ability to inspire teamwork and motivate staff within a matrix system
Excellent communication, planning, organizational, interpersonal, and problem-solving skills
Ability to work independently and negotiate and liaise with clients professionally
Good computer skills

Benefits

Comp & perks

Collaborative and inclusive environment
Growth and career development opportunities
Opportunity to learn and grow
Meaningful work contributing to life-changing therapies
Domestic and international travel opportunities