JUMP TO CONTENT

Project Coordinator

JR063602

About the role

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

Mapi Research Trust (MRT) is a non-profit organization dedicated to improving patients' quality of life by facilitating access to Patient-Centered Outcome (PCO) information. We promote scientific approaches in the PCO field and encourages exchanges between academics, pharmaceutical companies, and international organizations around the world in the service of incorporating the patient's voice into every step of the development process of new treatments, https://mapi-trust.org//
We are looking for a Project Assistant to join our MRT team in Lyon. In this role you will provide customers (Pharmaceutical companies, e-vendors and Academics from scientific community) information on instruments/COAs (Clinical Outcomes Assessment) via our platform searching for the relevant information in given timeline and utilizing various sources.

The primary responsibilities of this job include:

  • Centralization of data on instruments for yearly selection
  • Selection of instruments to include in PROQOLID found in various sources
  • Contact of instruments Developers
    • Identification of contact name and details
    • E-mailing
    • Follow-up
    • Answering to developers queries
  • Extraction of non-scientific data
    • For PROQOLID: Update and Quality check of non-scientific data for new or to be updated instruments
    • For Data Extraction projects (instrument descriptive grids)
  • Database handling of
    • Creation of instrument pages in the BackOffice & Inclusion of data collected (incl. those from author)
    • Final publication of questionnaires extracted
    • Technical support: Answering questions related to databases about user experience
  • Articles
    • Searching and ordering articles
    • Filing articles
    • Transfer of articles to PM
  • External Resources
    • Assist the Project Manager in the production follow-up: workload follow-up, planning and dispatch, delivery reception and reporting
  • DCP Unit administrative follow- up
    • Invoices/Budget/Time
  • Reporting: update of tables and monthly dashboards
  • Participating in the training program for new team members
To be successful you will have:
  • Strong customer service skills, including ability to communicate clearly and positively with clients (clarifying by questioning and reformulating) and resolve customer issues or complaints. The customer also being internal MRT users.
  • Ability to qualify and formulate the need and requirement
  • Ability to present information effectively, clearly, and concisely
  • Fluency in English (written/oral)
  • Search, find, evaluate relevance of, analyze, interpret, summarize, and compile data from various research sources
  • Prioritize and organize multiple simultaneous tasks to ensure timely and accurate completion. Requires effective use of organizational and time management skills. Ability to propose different scenarios according to the priorities
  • Work with minimal supervision and demonstrate appropriate initiative when making decisions and problem-solving. Demonstrate flexibility and an open-minded approach to task completion
  • Excellent ability to present information effectively, clearly, concisely and positively both orally and in writing (instructions, procedures, guidelines, work note, work documents, training session, marketing documents…)
  • Carry out instructions furnished in written or oral form, with attention to detail
  • Understand, apply, and use personal computers and various software applications (e.g. OUTLOOK, WORD, EXCEL, PowerPoint, Acrobat, etc.), and browse the Internet (visible and invisible web)
  • Effectively work independently, as well as part of a team and with a diverse group of individuals in an international context
  • Ability to maintain confidentiality of information regarding company financial and other information
  • Establish and maintain cooperative working relationships with others contacted in the course of work; teamwork and consensus-building skills, sharing of useful information and experience
  • Ability to spot issues related to projects or organization, propose corrections or escalate to management team
  • Experience with medical terminology and/or within research/clinical settings desirable
NEXT STEPS:
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
Mapi Research Trust and ICON Plc are equal opportunity employers - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment
List #1

Day in the life

Headshot of male
25 Years in Clinical Operations at ICON: Ricardo Cortizo Justo Q&A

Teaser label

Our People

Content type

Blogs

Publish date

04/08/2026

Summary

Ricardo Cortizo Justo, Director of Clinical Operations and Site Head for Paris at ICON plc, recently marked an exceptional milestone of 25 years with the organisation. Over the course of his career, R

Teaser label

Ricardo shares insights from 25 years at ICON, covering clinical operations, leadership, and career development.

Read more
Heartbeat vitals on monitor
Central Monitoring vs On Site Monitoring

Teaser label

Industry

Content type

Blogs

Publish date

04/03/2026

Summary

Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

Teaser label

Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

Read more
middle aged male wearing shirt
Francis' Journey back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/26/2026

Summary

Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

Teaser label

Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

Read more
View all

Similar jobs at ICON

Trial Delivery Management, Base

Salary

Location

US, Blue Bell (ICON)

Location

Burlington

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Project Management

Job Type

Permanent

Description

As a TDM at ICON, you will be responsible for leading and coordinate project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards.What You Will

Reference

JR148315

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Clinical Trial Liaison (Trilingual)

Salary

Location

Brazil, Sao Paulo

Location

Buenos Aires

Sao Paulo

Bogota

Lima

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Liaison

Job Type

Permanent

Description

We are currently seeking a Trilingual Clinical Trial Enrollment Liaison to join our diverse and dynamic team. As a Clinical Trial Enrollment Liaison at ICON, you will play a pivotal role in designing

Reference

JR145938

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
Senior Clinical Research Associate

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR148555

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
(Sr) Project Manager, Feasibility Site Activation

Salary

Location

Mexico, Mexico City

Location

Sao Paulo

Mexico City

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Project Management

Job Type

Permanent

Description

As a Project Manager, Feasibility and Site Activation (FSA) at ICON, you will be responsible for planning and manage Feasibility and Site Activation (FSA) activities for assigned clinical studies.What

Reference

JR148391

Expiry date

01/01/0001

Florencia  Borello Taiana Read more Shortlist Save this role
Clinical Research Associate, Sponsor Dedicated

Salary

Location

Canada, Montreal

Location

Montreal

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR148329

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
Clinical Research Associate, Sponsor Dedicated

Salary

Location

Canada, Montreal

Location

Montreal

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR148331

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above