SES Project Lead

🕒 September 8

🌐 Argentina, Brazil – Remote

infoinfo

⏰ Full Time

🟠 Senior

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Logo of IQVIA

IQVIA

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Collaborate with pre- and post-award stakeholders to coordinate, plan, and implement Site Enablement Solutions • Develop global Site Enablement Solutions delivery strategies, identify sites, execute agreed scope, and expand services as warranted • Determine internal team resourcing based on study needs • Develop and execute operational plans for larger, multi-region studies or programs • Develop and implement risk management plans to minimize impact on project objectives and deliverables • Establish study-specific expectations and timelines • Communicate with sponsors and project teams to implement and monitor Site Enablement Solutions • Provide proactive operational and tactical recommendations based on study performance • Collaborate with internal and external teams to deliver site adoption and quality resource placement within specified timelines • Establish collaborative project delivery with Patient and Site Centric Solutions teams, including patient recruitment and Direct to Patient Campaign teams • Schedule and facilitate internal study meetings • Represent Site Enablement Solutions at site- and sponsor-facing meetings to present strategy, rationale, and training • Own study KPIs and financial performance • Manage scope of work, objectives, deliverable quality, and other assigned project activities • Manage and oversee internal workflow management systems to ensure compliance • Perform other duties as assigned by management

🎯 Requirements

• Bachelor's degree in life sciences or related field • 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 • Ability to work with global projects and global teams

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