Clinical Trials Delivery Lead

IQVIA LLC

Durham, Northern (NC, KY)

Hybrid

USD 93,000 - 233,000

Full time

6 days ago
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Job summary

IQVIA LLC in Durham, North Carolina seeks a Clinical Lead to join the core project team delivering clinical studies and ensuring regulatory compliance. You will collaborate with clinical teams to meet recruitment targets and manage risks throughout study lifecycles.

The role requires 5+ years in clinical research, knowledge of GCP/ICH guidelines, and strong leadership and communication skills. You will work with stakeholders across functions and contribute to delivery strategy for proposals and

Qualifications

  • Bachelor's Degree in health care or other scientific discipline required.
  • 5 years clinical research/monitoring experience or equivalent combination of education, training and experience.
  • Requires basic knowledge of Project management practices and terminology.
  • Requires good knowledge of GCP/ICH regulatory requirements.
  • Requires understanding of clinical research industry and project finances.

Responsibilities

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP, protocol) and contract/SOPs.
  • Achieve recruitment targets and implement recruitment strategies.
  • Develop and manage the project risk mitigation plan and clinical risks lifecycle.
  • Ensure clinical quality delivery by monitoring standards and addressing quality issues.
  • Lead the clinical team and coordinate with Project Leaders and stakeholders to meet milestones.

Skills

Leadership
Communication
Problem solving
Organization
Time management

Education

Bachelor's Degree in health care or other scientific discipline

Tools

Microsoft Word
Excel
PowerPoint

Job description

IQVIA LLC in Durham, North Carolina seeks a Clinical Lead to join the core project team delivering clinical studies and ensuring regulatory compliance. You will collaborate with clinical teams to meet recruitment targets and manage risks throughout study lifecycles.

The role requires 5+ years in clinical research, knowledge of GCP/ICH guidelines, and strong leadership and communication skills. You will work with stakeholders across functions and contribute to delivery strategy for proposals and

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