Senior Clinical Project Manager, Oncology, IQVIA Biotech

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 Senior Project Manager with proven experience in Oncology clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management professional who thrives in a fast-paced environment and is passionate about advancing therapies in the CNS space. You will leverage your expertise to lead complex, multi-regional studies and ensure operational excellence while building strong client relationships.

Overview
As a Senior Project Manager at IQVIA Biotech, you’ll play a critical role in accelerating the delivery of clinical trials and improving patient lives by bringing new therapies to market faster. You will lead core project teams, ensuring successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role combines strategic leadership, operational excellence, and customer engagement to deliver high-quality results.

Key Responsibilities

• Lead bid defense presentations and contribute to study strategy development.

• Develop and implement integrated study management plans.

• Oversee planning and execution of medium to large, multi-regional clinical studies, ensuring speed, quality, and cost optimization.

• Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction.

• Build and lead cross-functional teams, driving collaboration and milestone achievement.

• Monitor project progress, manage risks, and resolve issues proactively.

• Ensure compliance with ICH GCP, local regulations, and company processes.

• Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities.

• Mentor and support team members, promoting continuous improvement and knowledge sharing.

Qualifications

• Bachelor’s degree in Life Sciences or related field.

• 7+ years of clinical research experience, including 4+ years in project management.

• Strong knowledge of clinical trial conduct, regulatory requirements, and therapeutic areas.

• Excellent leadership, communication, and negotiation skills.

• Proven ability to manage complex projects across geographies and functions.

• Proficiency in MS Office and project management tools.