JUMP TO CONTENT

Clinical Trial Manager-IVD/Pathology (US-Remote)

  1. United States
2024-111488
  1. ICON Strategic Solutions
  2. Clinical Trial Management

About the role

This vacancy has now expired. Please click here to view live vacancies.

Overview:


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 as an IVD Study Manager with Pathology experience. 

 


Responsibilities:

  • Leads the global study team with full accountability for the study with respect to quality, cost and timelines.
    • Develops study design for technical studies in coordination with internal/external experts and the development project team
    • Provides input to study synopsis prepared by CST for Clinical Utility and Clinical Performance studies and ensures that these Studies are planned and executed based on study synopsis with full responsibility for study protocol and study report
    • Ensures that all studies are planned, executed, monitored, closed out and documented in a competent and compliant way within the planned time frame and costs.
    • Ensures that the study results are continuously validated, assessed, clear recommendations drawn and communicated.
    • Oversight of data management processes, data quality and results, data base closure and reporting.
    • Ensures that data and reports which are necessary for the characterization, regulatory approval and marketing of the products have been agreed upon, made available and are documented in a timely fashion.
    • Ensures and is responsible that study results are presented or submitted for publication in alignment with publication plans
    • Planning of the study specific content and budget within the development project team and controlling the related agreed upon budgets during the study.
    • Managing study site and clinical study agreements
    • Delegation and oversight of tasks and work packages for internal and external collaborators within the study.
    • Planning, procurement, preparation and delivery of materials necessary for carrying out the study, in cooperation with the Study Support team.
    • Ensure compliance to all relevant safety and QM procedures in all studies.

 


Qualifications:

 

• Knowledge of applicable standards and regulations for clinical trial and lab conduct
• Proven oral and written communications skills
• Experience in all stages of international clinical study management, study protocol design, report writing and monitoring and leading local teams
• Proven planning, organizing, interpersonal and leadership skills
• Ability to work independently to make sound decisions and analyze and solve problems
• Demonstrated experience in computer skills to include Microsoft Word, Excel and basic templates
• Statistical knowledge
• Minimum - Bachelor's degree in medical technology, chemistry, biology or other science relevant field

 

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

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.

 

#LI-JK1

List #1

Day in the life

A picture of chemists on a superimposed periodic table
5 reasons why you should consider a career in Clinical Research

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/17/2025

Summary

Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are

Teaser label

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

Read more
Man with headphones on looking at a laptop
Tips to make a lasting impression in a video interview

Teaser label

Career Progression

Content type

Blogs

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv

Teaser label

Ace your virtual job interview with these proven video interview tips.

Read more
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
View all

Similar jobs at ICON

Clinical Trial Manager (CMO) - Post-Trial Access

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

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

Reference

2025-120316

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Clinical Trial Manager - Oncology

Salary

Location

Spain, Madrid

Department

Clinical Trial Management

Location

Madrid

Remote Working

Home or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu

Reference

JR131543

Expiry date

01/01/0001

Katty Barreto Maia Read more Shortlist Save this role
Clinical Trial Manager - sponsor dedicated (80%)

Salary

Location

Germany

Department

Clinical Trial Management

Location

Germany

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Clinical Trial Manager, you will be leading the Local Study Team(s) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines comply

Reference

2025-120391

Expiry date

01/01/0001

Roxana Rosca

Author

Roxana Rosca
Read more Shortlist Save this role
Clinical Trial Manager

Salary

Location

Germany

Department

Clinical Trial Management

Location

Germany

Remote Working

Office Based

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

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

Reference

2025-119955

Expiry date

01/01/0001

Sarah Cameron

Author

Sarah Cameron
Read more Shortlist Save this role
Local Study Associate Director

Salary

Location

Philippines

Department

Clinical Trial Management

Location

Philippines

Remote Working

Office Based

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Local Study Associate Director, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a well

Reference

2025-119854

Expiry date

01/01/0001

Sitti Lim

Author

Sitti Lim
Sitti Lim

Author

Sitti Lim
Read more Shortlist Save this role
Clinical Research Manager (Local Project Manager)

Salary

Location

Taipei

Department

Clinical Trial Management

Location

Taipei

Remote Working

Office Based

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

As a Clinical Research Manager (Local PM) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Working location: Client offic

Reference

2025-118837

Expiry date

01/01/0001

Sandy Tang

Author

Sandy Tang
Sandy Tang

Author

Sandy Tang
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above