Description
As an Associate Clinical Project Management Director at IQVIA, you will supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery, time and quality resulting in strong financial performance and customer satisfaction.
Role & Responsibilities
- Serve as the Principal (or Person) in Charge (PIC) for Cronos projects, providing overall leadership and accountability for project initiation, execution, and closeout.
- Oversee project governance, ensuring compliance with Cronos and IQVIA policies, SOPs, and regulatory requirements.
- Lead, mentor, and develop a team of Project Managers and Project Manager Analysts, providing guidance, support, and professional development opportunities.
- Allocate resources, balance workloads, and ensure optimal team performance across multiple projects.
- Facilitate project governance reviews, risk assessments, and issue escalation processes.
- Act as the primary point of contact for senior/executive management regarding project status, risks, and escalations.
- Ensure accurate and timely completion of project deliverables, including financial reconciliation, documentation, and archiving.
- Provide operational consultation on all aspects of the Cronos service offering.
- Drive process improvement initiatives and champion best practices in project management and operational excellence.
- Represent Cronos Study Operations in cross-functional initiatives and strategic planning.
- Support business development activities as needed, including proposal development and client presentations.
Required Knowledge, Skills, and Abilities
- Proven leadership and people management skills, with experience overseeing project teams.
- Strong knowledge of project governance, risk management, and compliance in a clinical research environment.
- Excellent problem-solving skills and attention to detail.
- Strong computer skills, including Microsoft Office applications; experience with project management tools (e.g., Smartsheet, SAP, SharePoint) preferred.
- Ability to build strong business relationships and influence stakeholders at all levels.
- Excellent written and oral communication skills.
- Ability to manage multiple priorities in a fast-paced, dynamic environment.
- Strong commitment to quality and continuous improvement.
Minimum Required Education and Experience
- Bachelor’s degree in life sciences, business, or related field (Master’s preferred).
- 7+ years of experience in clinical research, project management, or study operations, with at least 3 years in a leadership role.
- Demonstrated experience in project governance, process improvement, and team management.