Site Activation Manager – Sponsor Facing

🔥 0 minutes ago

🌐 United Kingdom, Serbia, +6 more countries – Remote

🇬🇧 United Kingdom – Remote 🇷🇸 Serbia – Remote 🇵🇹 Portugal – Remote 🇷🇴 Romania – Remote 🇭🇷 Croatia – Remote 🇬🇷 Greece – Remote 🇧🇬 Bulgaria – Remote 🇫🇷 France – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

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

• Provide strategic oversight and project management for global or multi-regional Site Activation activities • Lead start-up delivery from pre-award through activation and lifecycle maintenance in compliance with ICH-GCP, regulatory requirements, and project timelines • Develop and execute the Site Activation Management Plan aligned with study strategy and scope of work • Collaborate with internal teams, regions, and external stakeholders to ensure efficient study start-up execution • Oversee regulatory submissions, approvals, contracts, and essential document processes • Assess regulatory landscapes and contribute to regulatory intelligence and strategy • Identify risks and propose practical solutions to support study delivery and bid processes • Ensure accurate tracking, reporting, and maintenance of project systems, timelines, and documentation • Support business development, including bid defense and client engagement activities • Mentor and coach team members and contribute to continuous improvement initiatives • Build and maintain strong client relationships and support customer-facing activities

🎯 Requirements

• Bachelor’s degree in Life Sciences or related field • Minimum 5-7 years’ experience in clinical research, including 3+ years in a leadership role • Proven international project experience across multiple regions • Strong leadership and project management skills with ability to manage multiple priorities • Demonstrated ability to deliver projects on time, within scope, and budget • Excellent communication, negotiation, and stakeholder management skills • Ability to lead through others and maintain effective cross-functional relationships • Strategic thinking and problem-solving • Leadership and team development • Regulatory and clinical trial expertise • Stakeholder engagement and collaboration • Quality and compliance focus