Senior Clinical Project Manager

Location: Seoul, Republic of Korea

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Lead Study Management Teams and oversee clinical trials from feasibility and site selection through start-up, execution, database lock, and close-out.
• Partner with Trial Delivery Leaders, physicians, data managers, supply managers, CROs, country teams, and global vendors.
• Manage study timelines, enrollment, budgets, documentation, issue resolution, escalation management, and inspection readiness.
• Oversee CAPA management and GCP compliance across clinical trial programs.
• Lead clinical trial managers across insourced and outsourced studies and provide coaching and mentoring.
• Take on complex programs and additional responsibilities such as Champion or Therapeutic Area Expert assignments.

Requirements

• At least 8 years of clinical trial management experience in the pharmaceutical industry or a CRO.
• 3–4 years of global project management experience.
• Relevant therapeutic area experience.
• Strong leadership, project management, stakeholder management, and budgeting skills.
• Strong English communication skills are required.
• Ability to proactively identify and resolve budget issues autonomously with key stakeholders.

Culture & Benefits

• Full-time employment.
• Work on global and regional clinical trial programs.
• Collaboration with cross-functional teams, CROs, and international vendors.
• Opportunities to lead complex studies and mentor less experienced clinical trial managers.