# Associate Clinical Project Management Director

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Associate-Director--Study-Operations--Rater-Services_R1559985-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_bc485c1f-d22

## 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.

## Skills

### Required
- project management
- leadership
- clinical research
- risk management
- compliance
- Microsoft Office
- Smartsheet
- SAP
- SharePoint

### Nice to have
- Master’s degree
- experience with project management tools

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Associate-Director--Study-Operations--Rater-Services_R1559985-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)