Skip to the page

(Senior) Clinical Trial Associate - Hamburg

IconWorkdayGermany, Mannheim
Posted 2 OctFound 25 OctSeen 18 hours ago

Check your resume for this job's 15 skills, free. Then have AI tailor it.

Fit

The keywords the posting names, against what your resume says.

Add your resume to see which of its keywords you already have, and get a resume tailored to this posting. 10 a month, free.

The Posting

CTA, hybrid in Hamburg

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.

As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do:

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key responsibilities include:

  • Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
  • Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
  • Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
  • Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
  • Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile:

You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
  • Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
  • Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
  • Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
  • Willingness to travel as required (approximately 10%)
  • Fluency in German and English language

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Facts

Source
Workday
External id
JR161101
Location
Germany, Germany
Remote
Remote, from the posting
Employment
Full time
Posted
2 Oct 2026
First seen
25 Oct 2026, 22:05
Last seen
1 Nov 2026, 18:41
Status
Not yet added
Posting id
0b95249a-78f9-55a9-897e-04d9148ab479