Clinical Program Lead: Delivery & Impact

IQVIA; North Carolina; On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA is seeking a Project Lead to join its clinical trial delivery team in the United States. The role focuses on delivering clinical studies to meet contractual requirements using IQVIA SOPs, policies and solutions to drive operational excellence and strategic leadership with customers.

You will collaborate across pre-clinical, clinical, operations, CMC and regulatory groups, lead regional studies as needed, and build integrated study management plans to ensure successful study delivery with

Qualifications

• Bachelor’s Degree Life sciences or related field required.
• 8-10 years experience in biopharmaceutical industry with experience supporting product development teams.
• Strong understanding of drug development strategies across all critical product development disciplines.
• Knowledge of clinical trials conduct and regulatory requirements (ICH GCP).
• Excellent written and verbal English communication; strong presentation skills.

Responsibilities

• Collaborate with cross-functional groups to support milestone achievement and manage study issues.
• Participate in bid defense presentations with Business Development and may lead for smaller regional studies.
• Deliver and manage smaller, less complex regional studies.
• Develop integrated study management plans with the core project team.
• Execute clinical studies per contract while optimizing speed, quality and cost; ensure adherence to SOPs.

Skills

Leadership

Communication

Problem solving

Organization

Time management

Stakeholder management

Education

Bachelor’s Degree Life sciences or related field

Tools

MS Office

Job description

IQVIA is seeking a Project Lead to join its clinical trial delivery team in the United States. The role focuses on delivering clinical studies to meet contractual requirements using IQVIA SOPs, policies and solutions to drive operational excellence and strategic leadership with customers.

You will collaborate across pre-clinical, clinical, operations, CMC and regulatory groups, lead regional studies as needed, and build integrated study management plans to ensure successful study delivery with