# Clinical Project Manager - EMEA

**Company**: ICON Strategic Solutions
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Global-Study-Lead_JR152025?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_cde3df60-b9b

## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As a Clinical Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards.

**Responsibilities**

Your focus will be on coordinating project and program management delivery, resolving issues, and developing team capability in a sponsor-dedicated model environment. Key responsibilities include:

- Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.

- Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.

- Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.

- Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organisational objectives.

- Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.

**Requirements**

You will have solid project and clinical project management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:

- A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organisation.

- Bachelor's degree in health, life sciences, or other relevant fields of study.

- At least 10+ years of relevant experience in clinical trial management.

- Preferred: 2+ years of monitoring experience.

- Experience in managing complex or global trials is advantageous.

- Preferred: Experience in managing all trial components from start-up to database lock.

- Strong performer / executor of operational tasks with strong skills and experience in study delivery.

- Experience of working across multiple types of study designs.

- Demonstrates leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organisational objectives.

- Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.

- Fluency in English (reading, writing, speaking).

**Rewards & Benefits**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- Competitive base salary and performance related incentives.

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

## Skills

### Required
- Clinical Trial Management
- Project Management
- Leadership
- Communication
- Collaboration

### Nice to have
- Monitoring Experience
- Global Trials Experience
- Coaching/Mentoring
- Team Leadership

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Global-Study-Lead_JR152025?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)