SES Project Lead

Role Overview:

The Site Enablement Solutions team at IQVIA provides qualified clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry patient recruitment patient visits assessments and other tasks IQVIA is able to relieve the burden on trial sites and support our sponsors in completing their trials on time and within budget.

The goal of the Site Enablement Solutions Project Lead (SES PL) role is to optimize overall delivery of Site Enablement Solutionsthroughout the lifecycle of projects. The SES PL will also serve asinternal consultants to the IQVIA study team and/or sponsor presentprogressand updates to sponsor and manage overall delivery of our services on a project including managing the Site Enablement project budget.

Key Responsibilities

• Collaborate with pre- and post-award stakeholders to manage the coordination planning and implementation of Site Enablement Solutions.
• Develop global SiteEnablement Solutionsdelivery strategy in identifying sitesexecuting on agreed upon scopeandextending/expandingour 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 approachfor 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.
• Other duties as assigned by management.

Qualifications:

• 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 youll work with global projects and global teams.

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IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

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