JUMP TO CONTENT

Clinical Outsourcing Manager

  1. Any EMEA Location
2022-96678
  1. Clinical Monitoring
  2. ICON Strategic Solutions (FSP)

About the role

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

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.


Summary

 

The Outsourcing Manager will support the outsourcing and contracting needs of Global Medicines Development and Affairs (GMDA). This individual will be responsible for the generation, negotiation and execution of contracts including budget and legal terms. The individual will ensure that the contract terms and budget meet the needs of the business. This position may be required to work under tight timelines.

 

Responsibilities

  • Responsible for ensuring confidentiality agreements are executed as required.
  • Responsible for the contract negotiation and execution for vendors supporting a business owner.
  • Act as the contact with vendors for negotiation of the scope of work, study assumptions and budgets.
  • Work closely with legal and other relevant functional groups for review and escalation of contract and budget issues.
  • Support cross-functional relationships with GMDA, legal and finance.
  • Maintain contracts database.
  • Report status of contracts.
  • Perform follow-up activities for accounts payable issues as requested by functional groups.
  • Follow up or escalate vendor requests for payment information.
  • Perform other duties as required.

Education and Experience

  • Bachelor's degree is required
  • Life sciences or business experience is preferred
  • Minimum of 3 years experience in clinical development including clinical trial budget development experience
  • Minimum of 2 years experience in Outsourcing
  • Negotiation, organizational and communication skills are required

Benefits of Working in ICON:

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.

At 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.

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, 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.

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 tha

Teaser label

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

Read more
5 different images of lab technicians
How to become a Clinical Research Associate (CRA)

Teaser label

Our People

Content type

Blogs

Publish date

11/13/2024

Summary

How to Become a Clinical Research Associate:   A Step-by-Step Guide The clinical research industry is projected to reach $52.0 billion by 2026, growing at an impressive rate of 5.6% annually.

Teaser label

Explore the step-by-step guide on how to become a Clinical Research Associate (CRA).

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

Teaser label

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

Read more
View all

Similar jobs at ICON

Sr. Clinical Research Associate

Salary

Location

Illinois

Location

Illinois

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR150997

Expiry date

01/01/0001

Kaitlyn Lurker Read more Shortlist Save this role
Sr. Clinical Research Associate

Salary

Location

California

Location

California

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR150983

Expiry date

01/01/0001

Kaitlyn Lurker Read more Shortlist Save this role
Sr. Clinical Research Associate

Salary

Location

California

Location

California

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR150962

Expiry date

01/01/0001

Kaitlyn Lurker Read more Shortlist Save this role
Sr. Clinical Research Associate

Salary

Location

California

Location

California

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR150958

Expiry date

01/01/0001

Kaitlyn Lurker Read more Shortlist Save this role
Clinical Research Associate II

Salary

Location

Nebraska

Location

Nebraska

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will

Reference

JR149083

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Senior Clinical Research Associate

Salary

Location

South Carolina

Location

South Carolina

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR149081

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above