(Senior) Clinical Trial Associate - Hamburg
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 8h ago
The date the source published, not the day we noticed it (2026-10-02). Last seen at its source just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Germany
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $109.4k–135k/yr
Middle 50% of 20 listings that do state pay — Healthcare · all levels · EMEA · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 1h ago · last seen just now
- location not stated
The listing
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