Clinical Project Manager Jobs in Raleigh, NC (NOW HIRING)

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.

We are seeking a US-based Clinical Project Manager with proven experience in Oncology clinical trials to join IQVIA Biotech.

Overview

As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will serve as a key member of the core project team, ensuring the successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role blends strategic leadership, operational excellence, financial oversight, and customer partnership to drive highquality outcomes across regional and global studies.

Key Responsibilities

• Participate in bid defense presentations and contribute to study strategy development; may lead presentations for smaller or regional studies.

• Develop and implement integrated study management plans alongside the core project team.

• Lead the planning and execution of smaller or less complex regional clinical studies, optimizing speed, quality, and cost.

• Serve as a primary or backup point of contact for clients, fostering strong, collaborative customer relationships.

• Build, manage, and guide crossfunctional project teams, ensuring effective communication and milestone achievement.

• Monitor study progress, proactively manage risks, and drive timely issue resolution.

• Ensure adherence to ICH GCP, applicable local regulations, standard processes, and company policies.

• Manage project financials, including forecasting, scope management, revenue optimization, and identification of acceleration opportunities.

• Oversee vendor management activities when assigned.

• Support team development by mentoring less experienced project team members and contributing to a culture of continuous improvement.

Qualifications

• Bachelor's degree in Life Sciences or a related field.

• 5+ years of relevant clinical research experience, including at least 1 year of project management experience.

• Broad protocol and therapeutic knowledge; familiarity with the competitive landscape and ability to articulate the value of IQVIA solutions.

• Excellent communication and presentation skills

• Proven leadership capabilities, including decisionmaking, performance management, and crossfunctional collaboration.

• Strong problemsolving, planning, organizational, and prioritization skills.

• Ability to manage conflicting priorities while maintaining quality and accuracy.

• Proficiency in MS Office applications (Word, Excel, PowerPoint).

• Understanding of project financials, including budgets, forecasting, and contractual obligations.

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 athttps://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.