Global Clinical Project Lead

IQVIA Inc; Florissant (MO); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Biotech is seeking an experienced leader to oversee the planning, implementation and execution of contracted clinical studies. The role requires managing project teams, maintaining client relationships and ensuring adherence to SOPs, WFPs and regulatory standards.

You'll coordinate cross-functional activities, monitor study progress, and provide training and capability support. Domestic and international travel up to 20% may be involved, with a focus on delivering quality outcomes for

Qualifications

• Bachelor degree in a health-related field with 3+ years of clinical trial experience.
• At least 1 year of management experience; supervising staff preferred.
• Experience in clinical monitoring or data management.
• Excellent verbal and written communication and presentation skills.
• Ability to work independently within a matrix team; Word/Excel/PowerPoint proficiency.

Responsibilities

• Lead project teams on regional and global studies.
• Maintain positive client relationships and negotiate with clients.
• Ensure studies follow SOPs and timelines per contract.
• Identify trends and respond to client and team members.
• Develop early warning systems for obstacles and propose solutions.
• Define training requirements and ensure LMS/documentation compliance.
• Oversee staff activities and support managers with project delivery.
• Assist in capability and proposal defense presentations.
• Support contract execution and CIS documentation.
• Participate in performance appraisals of team members.
• Stay current with FDA, GCP and ICH guidelines.

Skills

Clinical research

Communication

Organization

Interpersonal skills

Multitasking

Independent work

MS Office

ICH GCP knowledge

Education

Bachelor degree health-related field

Management experience

Tools

Word

Excel

PowerPoint

EDC systems

Job description

IQVIA Biotech is seeking an experienced leader to oversee the planning, implementation and execution of contracted clinical studies. The role requires managing project teams, maintaining client relationships and ensuring adherence to SOPs, WFPs and regulatory standards.

You'll coordinate cross-functional activities, monitor study progress, and provide training and capability support. Domestic and international travel up to 20% may be involved, with a focus on delivering quality outcomes for