Do you have Global/Regional Study Start Up Site Identification and are
now looking to further develop, implement and execute Site identification
plans.
As Site
Identification Lead you will be accountable for the development of Site
Identification Plans. Working with the Study Start up, 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. Ensuring all sites proposed for
selection are of a high quality standard and meet all site profile, due
diligence and protocol specific site requirements. As a 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.
You will need
Global Site Identification experience, leading sponsor initiatives such as
kick-off meetings, bid defenses, project update and status calls, and other
communications. We ask that you have a Bachelor’s degree, project and
client interaction skills, and experience leading Site Identification
activities globally in a clinical research environment.
As a Site
Identification Lead, you would advance clinical trial Site identifications
activities by understanding the client objectives and assist in the development
of the Site Identification Plans through leading a team of Site Identification
Specialists (SIS’s) who have responsibility for Site
Identification. The successful candidate will show capability in the
areas of clinical trial operations, meeting Site Identification and ICON
guidelines, and displaying project management skills to optimize performance and
collaboration to ensure successful study outcomes.
To succeed you
will need a Bachelor’s Degree preferably in life sciences with great project
management skill set and understanding of Site identification processes in many
different countries along with experience in a clinical research environment
(preferable focusing on Site Identification Activity).