Smith and Nephew
StudySiteManagementSpecialist
Neural analysis suggests this role is
optimal for Mid candidates.
“Study Site Management Specialist at Smith and Nephew. Manage day-to-day study execution. Coordinate site management activities”
What They're Looking For.
Must Have
GCP
Nice to Have
3 years of relevant industry experience
What You'll Do.
Manage day-to-day study execution
Coordinate site management activities
Ensure successful study execution at site level
Develop and maintain professional relationships
Develop regional study documentation
Conduct regional vendor qualifications
Maintain vendor oversight
Utilize study management systems
Support budget planning
Ensure study activities comply with regulations
Develop knowledge of business units
Represent Global Clinical Research Operations
Liaise with local product teams
How You'll Work.
Team & Collaboration
Liaise with cross-functional study teams; Represent S+N as primary contact for study sites; Liaise with local product teams/stakeholders; Liaise with in country sales and marketing personnel
Process & Methodology
small projects, large projects
Full Job Description
**Study Site Management Specialist** Physical well-being is more than just body; it includes our minds and emotions. Smith and Nephew develops technology to break health barriers, empowering people from farmworkers to grandparents to accept limitless possibilities. Our purpose: Life Unlimited. This role will be involved in managing the day-to-day execution of S+N sponsored studies via execution of site and regional vendor activities. Function as a regional/site liaison working with cross-functional study teams. **What will you be doing?** * Developing SME responsible, with guidance, for the coordination of all site management activities from selection, preparation, activation, enrollment, follow-up, and closure in small projects or portions of large projects. * Ensure successful execution of studies at the site level via strong collaboration with study teams including but not limited to Clinical Study Management, Data Management, Clinical Research Associates, Clinical Trial Associates and applicable vendors. * Represents S+N as the primary point of contact for study sites, applicable vendors, and Clinical Trial Associates. Responsible for development and maintenance of these professional relationships. * Development of regional study documentation such as protocols/addendums, ICFs, and local ethics/regulatory documents. * With support, conduct regional vendor qualifications and maintain vendor oversight. * Ensure site quality via site training, site visits if applicable, compliance reviews, trending, corrective actions, and escalation. * Utilise study management systems to create and maintain oversight of site documentation, data entry/integrity, monitoring, statuses, milestones, issues, systems access, etc. * Support Clinical Study Management with applicable budget planning, budget accruals and payments. * Ensure study related activities are carried out in accordance with the appropriate regional regulations and GCP guidelines. This will usually be ICH GCP for medi
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