JUMP TO CONTENT

Clinical Study Manager II

  1. Groningen
JR124732
  1. ICON Full Service & Corporate Support
  2. Clinical Trial Management
  3. Office Based

About the role

This vacancy has now expired. Please see similar roles below...

Clinical Study Manager- Phase I Research

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The Clinical Study Manager II provides clinical trial management for in-house and outsourced studies, performs quality checks, protocol and document
development, and executes study delivery plans aligned with program goals and timelines. Based at ICON's Early Phase Clinic in Groningen, Netherlands.

What you will be doing

- Reviews and assesses the research protocol, clinic budget, case report forms, informed consent forms and study volunteer information. 
- Participates in the assessment, preparation and implementation of studies for the clinic to ensure a timely and high-quality study output.  
- Conducts feasibility analysis. Reviews availability and workload for study volunteers, practicability and required personnel. Creates risk analysis and contingency plans. Coordinates in- and outpatient visits.  
- Serves as liaison between all clinic groups and the applicable clinic management. Communicates any changes in scope and/or cost and escalates issues and/or major deviations. Serves as clinic contact for the study sponsor. 
- Prepares and reviews clinic documents.
- Ensures proper sampling, collection and transmission of research data samples. 
-Communicates any changes in scope and/or cost and escalates issues and/or major deviations. Serves as clinic contact for the study sponsor. 
- Monitors the study timelines and output by clinic staff according to protocol and internal procedures.  

Your profile

  • Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred.

  • Previous experience in clinical research, preferably within the CRO or pharmaceutical industry.

  • Understanding of clinical trial regulations, guidelines, and industry standards.

  • Strategic thinking and problem-solving abilities with a focus on driving results.

  • Excellent leadership and communication skills, with the ability to effectively manage cross-functional teams.

  • Fluent in Dutch and English

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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

List #1

Day in the life

A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Read more
women working on a laptop
What is the difference between a clinical trial manager and a clinical project manager?

Teaser label

Career Progression

Content type

Blogs

Publish date

02/17/2023

Summary

Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan

Teaser label

And which role is right for you?

Read more
A picture of holographic images coming out of an iPad
Are remote decentralised clinical trials the future?

Teaser label

Inside ICON

Content type

Blogs

Publish date

10/03/2022

Summary

In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe

Teaser label

In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics. This is subject to change with an increase in decentralised clinical trials (DCTs).

Read more
View all

Similar jobs at ICON

Clinical Study Lead

Salary

Location

United States

Department

Clinical Trial Management

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Clinical Study Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-114839

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Clinical Trial Manager

Salary

Location

United States

Department

Clinical Trial Management

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-115603

Expiry date

01/01/0001

Brendan Hoey

Author

Brendan Hoey
Read more Shortlist Save this role
Clinical Trial Manager

Salary

Location

Bulgaria

Department

Clinical Trial Management

Location

Bulgaria

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-115556

Expiry date

01/01/0001

Dariusz Sternlicht Read more Shortlist Save this role
Senior Associate Study Management

Salary

Location

United States

Department

Clinical Trial Management

Location

United States

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-115504

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Sr Study Manager - Oncology - Home Based (US/Canada)

Salary

Location

United States, Canada

Department

Clinical Trial Management

Location

Canada

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Sr Study Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-115019

Expiry date

01/01/0001

Monica Hawkins Read more Shortlist Save this role
Local Trial Manager Ireland

Salary

Location

Ireland

Department

Clinical Trial Management

Location

Ireland

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

Local Trial Manager homebased in Ireland In this role, you will lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out at a country level in accordance with ICH-G

Reference

2024-115553

Expiry date

01/01/0001

Elisabeth Trivic Read more Shortlist Save this role

Browse popular job categories below or search all jobs above