# Senior Project Manager

**Company**: IQVIA
**Experience**: senior
**Job type**: full-time
**Salary**: zł225,500.00 - zł418,600.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Senior-Clinical-Project-Manager--Renal--Obesity--MASH----Global-Study-Leadership---Poland_R1561296?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f9de7ee8-97a

## Description

As a Senior Project Manager at IQVIA, you will provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies.

You will lead large-scale, multi-regional studies focused on renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.

**Key Responsibilities**

- Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes

- Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes

- Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance

- Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success

- Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle

- Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments

**Requirements**

- Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline

- 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment

- Experience leading renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) global clinical studies is strongly preferred

- Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements

- Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance

- Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment

- Exceptional leadership, communication, problem-solving and decision-making skills

- Passion for advancing clinical research and improving patient outcomes

The potential base pay range for this role, when annualized, is zł225,500.00 - zł418,600.00.

## Skills

### Required
- clinical research
- project management
- ICH-GCP
- regulatory requirements
- leadership
- communication
- problem-solving
- decision-making

### Nice to have
- renal
- obesity
- MASH (Metabolic Dysfunction-Associated Steatohepatitis)

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Senior-Clinical-Project-Manager--Renal--Obesity--MASH----Global-Study-Leadership---Poland_R1561296?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)