Site Identification Manager
About the role
This vacancy has now expired. Please see similar roles below...
ICON is seeking a Site Identification Manager to be based in the UK - remote working will be considered for this role!
Oncology experience and global experience are required! We will consider candidates with a background in feasibility and study start up.
The Site Identification manager will be responsible for leading the Site Identification process for studies by being accountable/responsible for the development of Site Identification Plans (based on an approved country strategy), Site Profiles and Protocol Specific Site Requirements appropriate to the individual study needs and in alignment with sponsor requirements The Site Identification Manager will be responsible for ensuring all sites proposed for selection are of a high quality standard and meet all site profile, due diligence and protocol study specific requirements
This role will involve liaising with the Study Activation Lead, PM and CTMs on the study to ensure delivery of the study start up timelines in terms of initiated sites and First Patient In (FPI) milestones
Other responsibilities of this role will be to act as subject matter expert in Site Identification/Selection process for internal and external customers alike and to provide input to Team members, Project teams, Business Development and to Sponsors. Also to drive process improvement initiatives for Site Identification as assigned to drive effectiveness and productivity, while maintaining ICON’s competiveness.
The successful candidate will also work with and build strong strategic alliances with our Sponsors and oversee site identification delivery across the portfolio of studies with our strategic alliance partners. This will involve dealing with issue escalation and to help build client specific processes where necessary.
The candidate should have a good understanding of ICON systems, excel and site identification processes.
To succeed you will need:
A University degree in medicine, science, or equivalent, and a background in medicine, science or other relevant discipline.
Significant experience in site identification planning and at least 5 years’ international experience in clinical drug development across a broad range of therapeutic areas within the CRO/Pharmaceutical industry at a manager and / or project manager level.
You will be an Excellent communicator (both in written and spoken language) with well-developed negotiation skills and the ability to liaise successfully with senior management, clinical project teams, other ICON departments and clients.
You will be competent in MS Word, Excel and PowerPoint with highly developed organizational, problem solving and analytical skill, with the ability to prioritize time-sensitive tasks and work independently, to make decision and to progress projects.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Inside ICONContent type
BlogsPublish date
04/18/2024
Summary
Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis
Teaser label
IndustryContent type
BlogsPublish date
04/18/2024
Summary
Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials
Teaser label
IndustryContent type
BlogsPublish date
04/12/2024
Summary
Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ
Who we are
Similar jobs at ICON
Salary
Location
Shanghai
Department
Clinical Operations Roles
Location
Shanghai
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2024-109845
Expiry date
01/01/0001
Author
Lai "Jenny" ZhangAuthor
Lai "Jenny" ZhangSalary
Location
US, Salisbury, NC
Location
Salisbury
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Research Site Services
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
JR117424
Expiry date
01/01/0001
Author
Mitzi OvertonAuthor
Mitzi OvertonSalary
Location
Canada, Burlington
Department
Clinical Monitoring
Location
Burlington
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Requirements: 12+ months of monitoring experience as a CRA for a sponsor or CROOncology experience as a CRA Located in Ontario, Canada At ICON, it’s our people that set us apart. Our diverse teams ena
Reference
JR117798
Expiry date
01/01/0001
Author
Sarah WoodAuthor
Sarah WoodSalary
Location
Argentina
Department
Clinical Monitoring
Location
Argentina
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
The Study Start-Up Associate (SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in
Reference
2024-108919
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
US, San Antonio, TX, IDS
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
San Antonio
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Laboratory
Job Type
Temporary Employee
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
JR113018
Expiry date
01/01/0001
Author
Alexis HenryAuthor
Alexis HenrySalary
Location
Netherlands
Department
Clinical Monitoring
Location
Netherlands
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2024-109724
Expiry date
01/01/0001
Author
Vanessa VerdicktAuthor
Vanessa Verdickt