Author Relations Project Manager, Clinical Outcome Assessments
About the role
This vacancy has now expired. Please click here to view live vacancies.
| The Author Relations Specialist is responsible for the creation, development and maintenance of the relationship with the Authors of Clinical Outcome Assessments (COA) within the Author Collaboration Unit (ACU) within the Mapi Research Trust. Mapi Research Trust is a non-profit organization dedicated to improving patients’ quality of life by facilitating access to Patient-Centered Outcome (PCO) information. Mapi Research Trust promotes 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. We are looking this role to be based in one of our offices on the East Coast - with preference for Raleigh. The primary responsibilities of this job include: The development of new and existing relationships and collaborations with target authors (and/or appropriate organizations) according to the list of priority authors established by the Team Manager from the first contact until the signing of the contract as well as the setting up of the collaboration process before implementation with the operations. 1. Ensure the contact, negotiation and monitoring of target authors in order to offer them appropriate services (Translatability assessment, webinars, articles in the PRLNL, authors reports ...) in exchange for distributing their questionnaires (original, translation in print and electronic versions of the license) by MRT and a translation by Mapi exclusive VL. 2. Write collaboration agreements between MRT and the authors according to the existing model, adapting it to the context if needed. 3. Ensure the implementation of contracts by operations department according to the authors by adapting existing models in context with the support of the legal filing Mapi. 4. Supervise set up processes as agreed with Authors before implementation Project Management Manage (or provide support in the management of) various sized ACU projects from beginning to end including budget, dashboards, organizational and administrative aspects, ensuring deadlines are met or exceeded and signing off on completed project Travel, Marketing, Communication Participation in the establishment of appropriate marketing tools for ACU related activities Participation in ACU related communication as set forth in the ACU strategy. May attend industry and academic functions, such as association events and conferences, and provide feedback and information on market and creative trends to Mapi Marketing team. May engage in appropriate travel to meet with instrument developers and or appropriate organizations to develop author relationships. |
| Other Participate in developing and monitoring the Trust’s objectives and performance metrics Participate in liaising with all Mapi departments to establish and maintain cross-departmental relationships, synergies, procedures, and efficiencies. Responsible for promoting and fostering professional and collegial internal and external client, expert and author relationships. Participate in providing input and oversight for enhancement of tools used by the Trust and Mapi in relation to ACU. Participate in developing and maintaining Standard Operating Procedures related to the Trust, for representing the Trust in sponsor audits and for implementing corrective or preventive actions for Trust issues or audit findings. Participate in the improvement of the Quality Assurance System. Complete other appropriate duties, as assigned by the manager, which require similar skills in accordance with business needs. |
| Essential Criteria: |
|
|
| Benefits of working at ICON: Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, and life assurance and staff recognition schemes. We also have a defined career path for successful individuals in this practice. What’s Next? 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. ICON plc Company is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment. |
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
Similar jobs at ICON
Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clin
Reference
JR138841
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
US, Blue Bell (ICON)
Department
Clinical Trial Management
Location
Blue Bell
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team. As the Senior Clinical Trial Manager, you will hold a crucial role in ensuring the successful delivery of
Reference
JR139027
Expiry date
01/01/0001
Author
Michael HartleyAuthor
Michael HartleySalary
Location
Regional United States (PRA)
Location
Multiple US Locations
Mechelen
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Medical Writing
Job Type
Permanent
Description
We are currently seeking a Senior Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medi
Reference
JR138977
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
US, Naperville, Illinois
Location
Texas
Missouri
Naperville
Chicago, IL
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What you will be doing:Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internat
Reference
JR138844
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
UK, Warwickshire
Department
Accellacare Site Network
Location
Warwickshire
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Nursing
Job Type
Permanent
Description
This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ne
Reference
JR136410
Expiry date
01/01/0001
Author
Jenny DowningAuthor
Jenny DowningSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. You will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulat
Reference
JR136057
Expiry date
01/01/0001
Author
Florencia Borello TaianaAuthor
Florencia Borello Taiana