Senior Director Site Networks Mobilization Lead
About the role
This vacancy has now expired. Please click here to view live vacancies.
About the Senior Director, Site Network Mobilization Lead role within ICON:
Home based in the US or Europe
The Senior Director, Site Network Mobilization Lead will primarily be responsible for the project management, process oversight and timelines for expanding the Global Site Network business across EMEA and the US. Strong collaboration, project management and change management skills are required to support the identification of new site targets and onboarding those sites into the Global Site Network.
Benefits of working at ICON:
We will provide our Senior Director, Site Network Mobilization Lead with the resources to be successful in supporting their line of business. In addition, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.
Responsibilities:
- Drive identification and adoption of new sites /PI's into the ICON Global Site Network based on overall GSN expansion plans
- Support the on-boarding of new site targets in key EMEA/US for incorporating into ICON Global Site Network with the relevant Due Diligence teams
- Develop overarching Global Site Network process optimization strategic plan including review existing SOPs, operating guidelines and process usage across current Global Site Network operations and drive the process harmonization to enable high performing, top quality sites.
- Work with the assigned training leads for a scalable role based training solution across the Global Site Network
- Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
- Support the Company's culture and values by promoting an honest and trustful working environment.
- Develop excellent client relationships, customer service and customer experience by actively monitoring customer satisfaction.
- Ensures departmental compliance with SOPs. And ensures relevant SOPS are integrated with other functions as appropriate.
- Conduct professional client discussions on solutions to challenges the customer is experiencing using ICONs Site Networks & training solutions and other resources provided by ICON.
- Travel (approximately 30%) domestic and/or international.
To succeed you will need:
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- US/LATAM/CAN- At least 10 years of experience in clinical drug development.
- EU/APAC- Strong experience in clinical drug development and significant proven experience in applying customer solutions in clinical research.
- Demonstrable experience of customer and stakeholder relationship management with a client focused approach to work.
- Possesses executive presence. Capable of establishing immediate credibility with business partners internal and external to ICON to build consensus and achieve goals through influence and negotiations.
- Ability to prioritize and manage multiple responsibilities simultaneously.
- Proven track record at managing large scale change management programs.
- Must have excellent interpersonal and communication skills, preferably practiced in an international clinical research environment.
- Experienced in delivering presentations at conferences, client meetings and training sessions.
- Ability to liaise and work well with professionals across departments including executive management, senior functional leaders and clinical project teams.
- Ability to work in a matrix environment and to value the importance of teamwork and collaboration.
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.
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
Turkey, Ankara
Department
Clinical Monitoring
Real World Solutions
Location
Ankara
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As a CSA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, c
Reference
JR137245
Expiry date
01/01/0001
Author
Jacek JaworskiAuthor
Jacek JaworskiSalary
Location
Turkey, Ankara
Department
Clinical Monitoring
Location
Ankara
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking an In-House Clinical Research Associate to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of c
Reference
JR130319
Expiry date
01/01/0001
Author
Jacek JaworskiAuthor
Jacek JaworskiSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Supplies
Job Type
Permanent
Description
We are currently seeking a Manager, Clinical Supplies to join our diverse and dynamic team. As a Manager, Clinical Supplies at ICON, you will play a pivotal role in overseeing the management and distr
Reference
JR138594
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Office or Home
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
JR137821
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
China, Shanghai
Department
Clinical Monitoring
Location
Shanghai
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Job Advert PostingWe are currently seeking a Senior Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal ro
Reference
JR131213
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
West Point, PA
Location
West Point, PA
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Logistics & Supplies
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Supply Associate to join our diverse and dynamic team. As a Senior Clinical Supply Associate at ICON, you will play a crucial role in managing and overseeing
Reference
JR138975
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon Pupek