Global Clinical Project Lead

IQVIA Inc; Overland Park (KS); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA Biotech in Overland Park, KS seeks an experienced clinical trial program manager to plan, implement and execute contracted activities across regional and global studies. You will lead project teams, maintain client relationships and ensure timelines meet contract requirements.

You will collaborate with management to develop standards, training, and process improvements while complying with FDA, ICH-GCP guidelines and SOPs. Domestic and international travel up to 20% may be required.

Qualifications

• Bachelor-level or equivalent in a health-related field.
• Minimum three years clinical trial experience in CRO or related org; one year of management experience.
• Experience in communication, documentation and project coordination.

Responsibilities

• Manage full scope regional and global projects.
• Lead project teams and maintain client relationships.
• Negotiate with clients to ensure processes are maintained and within scope.
• Ensure projects run per SOPs and contract timelines.
• Develop training requirements and assist with process improvements.
• Maintain knowledge of FDA, GCP and ICH guidelines.

Skills

Clinical research knowledge

Project management

Client relationship management

Communication skills

Organizational skills

Team leadership

MS Office

Education

Bachelor's degree in health-related field

Tools

Word

Excel

PowerPoint

Electronic data capture

Job description

IQVIA Biotech in Overland Park, KS seeks an experienced clinical trial program manager to plan, implement and execute contracted activities across regional and global studies. You will lead project teams, maintain client relationships and ensure timelines meet contract requirements.

You will collaborate with management to develop standards, training, and process improvements while complying with FDA, ICH-GCP guidelines and SOPs. Domestic and international travel up to 20% may be required.