Senior Clinical Project Lead: Trials Delivery

IQVIA LLC; Durham (NC); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA LLC in the United States seeks a Project Lead to drive clinical study delivery, liaising with clinical teams to accelerate drug development while ensuring quality and compliance with SOPs. You will lead study teams, manage budgets, risks, and stakeholder communications to meet contractual requirements.

This role requires a life sciences degree, 5+ years in project management, strong English communication, and the ability to collaborate across functions.

Qualifications

• Bachelor's degree in life sciences or related field required.
• 5+ years relevant experience including at least 1 year in project management.
• Knowledge of clinical trials and regulatory requirements (ICH GCP).
• Strong English communication and presentation skills.
• Ability to lead cross-functional teams and manage budgets.

Responsibilities

• Participate in bid defense presentations with Business Development.
• Delivery and management of smaller regional studies.
• Develop integrated study management plans.
• Execute studies per contract while optimizing speed, quality and cost.
• Set objectives of the core project team and assess performance.
• Collaborate with other functional groups to hit milestones and manage issues.
• Monitor progress and report to stakeholders internally and externally.
• Manage risk and lead problem solving and resolution efforts.
• Ensure project quality and implement corrective actions.
• May serve as primary contact with customer and manage vendor relationships.
• Build cross-functional team and ensure timely delivery.
• Ensure financial success and forecast opportunities.

Skills

Communication

Leadership

Problem solving

Time management

Cross-functional collaboration

Financial acumen

Education

Bachelor's Degree Life sciences or related field

Tools

MS Office

Job description

IQVIA LLC in the United States seeks a Project Lead to drive clinical study delivery, liaising with clinical teams to accelerate drug development while ensuring quality and compliance with SOPs. You will lead study teams, manage budgets, risks, and stakeholder communications to meet contractual requirements.

This role requires a life sciences degree, 5+ years in project management, strong English communication, and the ability to collaborate across functions.