Project Manager

This is a fully remote position, open to applicants in South Korea.

📋 Description

• Oversee one or more assigned Phase I through IV clinical trials, which may be local, regional, or global in nature.

• Coordinate and manage clinical trials from initiation through to close-out activities.

• Direct the technical, financial, and operational components of projects.

• Collaborate with functional area leads to assess and evaluate project requirements, interpret complex data, and implement contingency or rescue strategies.

• Ensure project deliverables align with customer expectations regarding time, quality, cost, and contractual obligations.

• Lead core project team members and facilitate the leadership of extended or complete project teams.

• Direct internal and external cross-unit coordination, including subcontractors.

• Define and manage project resource requirements and develop contingency plans.

• Design, implement, monitor, and revise project plans as necessary.

• Foster teamwork and address conflicts effectively.

• Communicate project-related information to Project Management leadership.

• Achieve financial performance objectives for assigned clinical projects.

• Initiate enhancements to improve work efficiency and quality.

• Serve as the primary client contact and nurture strong client relationships.

• Ensure project personnel are trained on protocols and study processes, adhering to professional standards, SOPs, GCP, and local regulations.

• Identify training and development needs and contribute to performance evaluations.

• Manage delegated responsibilities of designated projects.

• Perform additional tasks as assigned by management.

⛳️ Requirements

• University or college degree (preferably in life sciences) or certification in a related allied health profession from an accredited institution, or an equivalent mix of education and experience.

• At least five (5) years of experience in the clinical pharmaceutical industry, showcasing demonstrated skills and proficiency in clinical project management tasks.

• Alternatively, over five (5) years of supervisory experience in a healthcare setting and four (4) years of clinical research experience in the pharmaceutical or CRO industries, or proven relevant clinical development experience and skills.

• Comprehensive understanding of project management processes.

• In-depth knowledge of ICH Guidelines and GCP, including international regulatory standards for clinical development programs.

• Willingness to travel domestically and internationally, including overnight stays.

• A valid current passport is required.

• Must possess a valid driver's license and the ability to drive.

• Proficient in the local office language and English, both written and verbal.

• Extensive knowledge of the drug development process and client requirements.

• Proven ability to manage projects in a multi-office environment.

• Capable of handling multiple competing priorities and utilizing resources effectively.

• Ability to inspire teamwork and motivate staff within a matrix structure.

• Exceptional communication, planning, organizational, interpersonal, and problem-solving abilities.

• Ability to work independently and negotiate professionally with clients.

• Strong computer skills.

🏝️ Benefits

• Collaborative and inclusive workplace environment.

• Opportunities for growth and career development.

• Chance to learn and advance professionally.

• Engaging work that contributes to transformative therapies.

• Opportunities for domestic and international travel.