Global Clinical Project Lead - Trial Delivery & Clients

IQVIA Inc; Abingdon (VA); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Inc. is seeking a capable project leader to manage regional and global clinical study programs. You will guide study teams, ensure contractual scope compliance, and maintain strong client relations while upholding FDA, GCP, and ICH standards.

The role requires experience in clinical trials, excellent communication, and the ability to travel domestically and internationally as needed. You will collaborate with cross-functional teams to drive timelines and quality in a fast-paced environment.

Qualifications

• Bachelor degree in a health-related field with 3+ years direct clinical trial experience.
• Experience managing people in a scientific/clinical environment preferred.
• Clinical Monitoring or Data Management experience required.
• Excellent verbal and written communication and presentation skills.
• Ability to travel domestically or internationally as required.
• Working knowledge of Word, Excel, and PowerPoint required.

Responsibilities

• Oversee full-scope regional and global study projects and lead project teams.
• Build and maintain positive client relationships and ensure project delivery within scope.
• Negotiate with clients to maintain IQVIA Biotech processes.
• Review study trends and respond proactively to clients and teams.
• Develop training requirements and ensure study-specific compliance.
• Ensure SOPs and work practices align with contracts and timelines.
• Support capability development and proposal presentations.
• Maintain FDA, GCP, and ICH knowledge and ensure quality.

Skills

Strong communication skills

Organizational skills

Positive attitude

Interpersonal skills

Multitasking

Independent reasoning

Baseline targets tracking

Data processing basics

ICH GCP knowledge

Education

Bachelor's degree in health-related field

Equivalent education/experience

Tools

Word

Excel

PowerPoint

Job description

IQVIA Inc. is seeking a capable project leader to manage regional and global clinical study programs. You will guide study teams, ensure contractual scope compliance, and maintain strong client relations while upholding FDA, GCP, and ICH standards.

The role requires experience in clinical trials, excellent communication, and the ability to travel domestically and internationally as needed. You will collaborate with cross-functional teams to drive timelines and quality in a fast-paced environment.