About The Position

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Join a team driving innovation in Immuno-Oncology and Cell & Gene Therapy clinical research. We are seeking an experienced Associate Clinical Project Management Director to lead the strategic planning, execution, and delivery of complex global clinical trials while ensuring exceptional quality, customer satisfaction, and financial performance.

Requirements

  • Bachelor's degree in Life Sciences or a related field.
  • 10+ years of clinical research experience, including 6+ years of project management experience.
  • Direct experience in Immuno-Oncology and Cell & Gene Therapy clinical trials is required.
  • Strong knowledge of ICH-GCP, clinical trial regulations, and global study management.
  • Proven ability to lead cross-functional teams, manage sponsor relationships, and drive successful project delivery.
  • Excellent communication, leadership, financial management, and problem-solving skills.

Responsibilities

  • Lead and oversee global clinical studies and programs from start-up through closeout.
  • Serve as the primary contact for sponsors, building strong client relationships and providing strategic project leadership.
  • Drive study delivery by managing timelines, budgets, resources, risks, and quality outcomes.
  • Lead cross-functional teams to ensure operational excellence and successful milestone achievement.
  • Support business development activities, including proposal strategy and bid defense presentations.
  • Proactively identify and mitigate study risks, oversee issue resolution, and manage change control processes.
  • Mentor and develop project team members while fostering collaboration and continuous improvement.

Benefits

  • Incentive plans
  • Bonuses
  • Health and welfare benefits
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