PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

In an industry where cost-cutting and layoffs are common, PSI stands out as a stable and secure workplace. Our dedication to stability is evident in our exceptionally high repeat and referral business rate and minimal staff turnover. Many of our colleagues have been with us for over 15 years, contributing to our long-standing traditions and history. 

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

In this role, you will be entrusted with the critical task of managing PSI operational presence in South Korea and will be responsible for all aspects of operational and strategic management.

Location: Seoul, South Korea

The scope of responsibilities encompasses the following crucial functions:

• Propose country development strategy, lead the planning and execution of Clinical Trials in the country.
• Set country growth objectives in line with corporate objectives.
• Ensure smooth daily operations of the company in Japan. Oversee corporate and project-related progress in South Korea.
• Communication point to investigators, regulatory and ethics authorities, clients and vendors for various project-related matters.
• Line management of staff in South Korea.
• Coordination of resource allocation to projects and utilization monitoring.
• Oversight of the staff workload, performance appraisal and career advancement.
• Training, coaching and mentoring the team.
• Hiring, onboarding and integrating new employees.
• Ensuring compliance with GCP standards and internal/external procedures.
• Development and implementation of quality control.
• Management of the budgets on the country level.

The ideal candidate for this critical role must possess:

• College or University degree in Life Sciences
• Demonstrated Operations experience in a CRO (preferable), or a pharma company
• Experience with clinical research sites, R+D processes, legal, regulatory and ethics in Japan
• At least 10 years’ experience in Clinical Research
• Experience in people management and leadership
• Bid defense experience is preferable
• Financial knowledge and demonstrated ability to manage budgets
• Excellent English
• Communication and negotiations skills
• Proficiency in standard MS Office applications
• Ability to travel internationally
• Strong time management, organizational, leadership, planning and presentation skills, result-oriented approach

The successful candidate will be expected to uphold the highest standards of professionalism and contribute significantly to the company's growth and success in the Korean market. 

Make the right call and take your career to a whole new level, where quality is the cornerstone of your work and training.  If shortlisted for an interview, our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.  We will guide and support you with information, making your interview experience smooth and comfortable.