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IQVIA

Associate Clinical Project Management Director, Immuno-oncology, IQVIA Biotech

Posted Yesterday
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In-Office
Durham, NC
103K-286K Annually
Expert/Leader
In-Office
Durham, NC
103K-286K Annually
Expert/Leader
Leads complex global immuno-oncology and cell and gene therapy clinical trials from start-up through closeout. Manages timelines, budgets, resources, risks, quality, and change control while serving as the primary sponsor contact. Oversees cross-functional teams, supports proposals and bid defenses, resolves issues, and mentors project staff. Requires extensive clinical research and project management experience, therapeutic expertise, global study knowledge, and strong leadership and communication skills.
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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.

Key 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.

Required Qualifications

  • 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $102,500.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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