JUMP TO CONTENT

TMF Specialist I

JR089708

About the role

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

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

As a TMF Specialist I/II you will complete Document Management activities in support of client services contracts and internal ICON business needs.

What you do?

  • Process study documents in accordance with client and study requirements as per study-specific processes, ICON SOPs/WPs and regulations, where applicable.

  • Liaise with study teams and other TMF staff in order to fulfill job responsibilities and activities.

  • Complete departmental projects as assigned in accordance with specified timelines, ICON SOPs/WPs and regulations.

  • Maintain study files as per study and/or client requirements or in accordance with ICON SOPs/WPs and applicable regulations.

  • Complete activities related to document receipt and processing which may include but is not limited to: document receipt and review, scanning and indexing, quality control, copying, filing, forwarding or return to client/study teams and archiving.

  • Provide information necessary to complete client and/or departmental status reports as requested by the management of TMF department.

  • Inform the Manager of training issues, project activities, quality issues and timelines as directed.

  • Provide copies of study documents to ICON or client personnel as requested.

  • Participate in client and/or ICON audits and document archiving activities as necessary.

  • Participate in training related to fulfillment of responsibilities as required by ICON and/or the client.

  • Liaise with Clients, as appropriate, on project issues when directed by the Manager.

  • Handle special projects or duties as requested by the Manager.

What you need?

  • Must have 0-2 years of knowledge/experience in Excel VBA. Ability to successfully liaise with study project teams, staff, clients and management, as necessary.

  • Good oral and written communication skills and interpersonal skills.

  • Bachelors Degree in Life Science preferred

Why join us:

Ongoing development is vital to us, and as a member of our team you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. We offer a very competitive salary and benefits package that includes an excellent recruitment plan, health coverage, paid time off, income protection insurance programs, and staff recognition schemes.



Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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 through the form below.

List #1

Day in the life

Headshot of male
Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish date

12/10/2025

Summary

Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.

Teaser label

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

Read more
Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
View all

Similar jobs at ICON

Senior Specialist Publications Operations

Salary

Location

Mexico, Mexico City

Location

Montreal

Mexico City

Prague

Dublin

Milan

Madrid

Reading

Gdansk

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Senior Site Management Associate to join our diverse and dynamic team. As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site manage

Reference

JR140159

Expiry date

01/01/0001

Rita Villavicencio Read more Shortlist Save this role
Senior CRA - Oncology - West/Southwest

Salary

Location

Las Vegas, NV

Location

Portland

New Mexico

Seattle, WA

Dallas, TX

Houston, TX

Las Vegas, NV

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR140709

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Pharmaceutical Copywriter

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Patient Recruitment

Job Type

Permanent

Description

We have an incredible opportunity for a versatile and strategic Copywriter to join ICON’s Patient Recruitment Solutions (PRS) digital team. The Copywriter will develop compelling copy for clinical tri

Reference

JR133551

Expiry date

01/01/0001

Tallulah Pierre Read more Shortlist Save this role
Clinical Research Coordinator Nurse

Salary

Location

Ames, IA

Department

Accellacare Site Network

Location

Ames, IA

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Nursing

Job Type

Permanent

Description

We have an incredible opportunity for a Clinical Research Coordinator Nurse (CRC Nurse) to join ICON’s Accellacare team. The CRC Nurse is responsible for completing trial assignments in an autonomous,

Reference

JR135083

Expiry date

01/01/0001

Lauren Berretta Read more Shortlist Save this role
Research Scientist

Salary

Location

US, Lenexa KCIB (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Research and Development

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR139132

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
Laboratory Proj Coordinator I

Salary

Location

Mexico, Mexico City

Department

Full Service - Development & Commercialisation Solutions

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Project Management

Job Type

Permanent

Description

JR114567Laboratory Proj. CoordinatorSite: Mexico, Mexico CityAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil o

Reference

JR137281

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above