Clinical Trial Manager

ICON; Deutschland; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

As a leading Clinical Trial Manager at ICON, you will oversee all clinical aspects of trials in a dynamic environment. Utilizing your expertise in Medical Devices, you will manage clinical resources, budgets, and cross-functional collaboration to ensure successful study outcomes. ICON offers a competitive salary and diverse benefits focused on employee well-being, making it an exciting opportunity for passionate professionals in clinical research.

Leistungen

Annual leave entitlements

Health insurance options

Retirement planning

Global Employee Assistance Program

Life assurance

Childcare vouchers

Bike schemes

Gym discounts

Travel passes

Qualifikationen

• At least 7 years of experience in clinical studies.
• Proven ability to deliver clinical study outcomes.
• Willingness to travel up to 20%.

Aufgaben

• Oversee the clinical budget and develop monitoring plans.
• Liaise with sponsors and vendors, identify and mitigate risks.
• Lead clinical resources and set expectations for the study team.

Kenntnisse

Fluent in German

Fluent in English

Clinical study management

Technical expertise in Medical Devices

Ausbildung

Four-year degree or equivalent education

Jobbeschreibung

As a Clinical Trial Manager, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. You will work dedicated to the sponsor and will be responsible for delivering all clinical aspects of the study.

What you will be doing:

• Responsible for the delivery of all clinical aspects of the study
• Oversee the clinical budget, develop monitoring plans and tools, train CRAs, drive enrollment and study start-up activities, review trip reports, implement corrective and preventative actions, liaise with the sponsor, vendors, and cross-functional teams, identify and mitigate risks, and report on clinical activities
• Participate in sponsor, investigator, and bid defense meetings
• Lead clinical resources in a matrix environment, including Clinical Trial Assistants and Clinical Research Associates
• Set expectations for the study team and promote a performance-oriented culture

Qualifications:

• At least 7 years of experience in clinical studies, with prior monitoring experience and within Medical Devices
• Four-year degree or equivalent education and experience
• Proven ability to deliver clinical study outcomes
• Expertise in the designated therapeutic area
• Willingness to travel up to 20%
• Fluent in German and English, both written and verbal
• Ability to attend client offices in Munich as needed

What ICON offers:

We prioritize building a diverse culture that rewards high performance and nurtures talent. Along with a competitive salary, we offer various benefits focused on well-being and work-life balance, including:

• Annual leave entitlements
• Health insurance options
• Retirement planning
• Global Employee Assistance Program
• Life assurance
• Optional benefits such as childcare vouchers, bike schemes, gym discounts, and travel passes

Visit our careers site to learn more: https://careers.iconplc.com/benefits

ICON is committed to inclusion and diversity, providing an accessible environment for all candidates. We consider all qualified applicants equally and provide reasonable accommodations upon request.