Clinical Project Manager

ICON Strategic Solutions; España; Remote; EUR 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Flexible benefits

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Project Manager to coordinate delivery across the EMEA region in a sponsor-dedicated model. You will drive project plans, budgets, and cross-functional collaboration to meet timelines and quality goals.

The role requires strong leadership, extensive clinical trial management experience, and the ability to manage global studies from start-up through database lock. Remote opportunities are available in multiple locations.

Qualifikationen

• 4+ years of experience in Clinical Trial Management
• Bachelor's degree in health, life sciences, or related field
• At least 10+ years of relevant experience in clinical trial management
• 2+ years of monitoring experience (preferred)
• Experience in managing complex or global trials is advantageous
• Experience in managing all trial components from start-up to database lock (preferred)
• Demonstrates leadership in motivating and empowering teams
• Experience coaching/mentoring CTMs and leading a team
• Fluency in English (reading, writing, speaking)

Aufgaben

• Developing and managing detailed project plans, timelines, budgets, and resources to ensure project delivery
• Leading cross-functional project teams and ensuring effective communication and collaboration
• Monitoring progress, identifying risks and issues, and implementing mitigation strategies
• Engaging with stakeholders to manage expectations and align with goals
• Preparing and presenting project reports and performance metrics to senior management

Kenntnisse

Clinical project management

Project coordination

Team leadership

Ausbildung

Bachelor's degree in health or life sciences

Jobbeschreibung

Clinical Project Manager - EMEA Several locations - Remote - Sponsor Dedicated

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

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What You Will Do

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

Your Profile

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 Organization.
• 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 organizational objectives
• Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
• Fluency in English (reading, writing, speaking)

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here