and post-award stakeholders to manage the coordination, planning, and implementation of Site Enablement Solutions.
Develop global Site Enablement Solutions delivery strategy in identifying sites, executing on agreed upon scope and extending/expanding our services as warranted.
Determine internal team resourcing based on study needs.
Develop and execute operational plans on larger, multi
region studies or programs, including develop and implement risk management plans for minimizing impact on project objectives and deliverables.
Establish study specific expectations and timelines.
Communicate with sponsors and project teams to implement and monitor impact of Site Enablement Solutions.
Provide ongoing proactive operational and tactical recommendations as needed based on study performance.
Collaborate with internal and external teams to deliver site adoption and quality resource placement within specified timelines.
Establish a collaborative approach for project delivery with Patient and Site Centric Solutions teams, including patient recruitment team and Direct to Patient Campaign.
Schedule and facilitate internal study meetings.
Represent Site Enablement Solutions at site/sponsor-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, and training.
Ownership for study KPI and financial performance.
Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects.
Manage and oversee internal workflow management systems to ensure compliance.
Requirements
Bachelors degree in life sciences or related field.
Experience requires 3
5 years of prior relevant experience: 5 years’ clinical trial experience
3 years’ experience at a CRO or clinical trial services provider
3 years in a Project Manager role
Advanced level of English, you'll work with global projects and global teams.