Global Site Activation Manager, Sponsor Dedicated (Slovakia)

About the role

iQVIA is looking for a Global Site Activation Manager, sponsor dedicated, based in Bratislava. The role leads the strategic, operational and financial delivery of site activation across assigned studies and regions, accelerating site activation to support timely patient enrollment. It covers site identification and selection, ethics and regulatory submissions, and site contracting in line with sponsor and company requirements. The position is home-based.

Key responsibilities

• Provide strategic oversight and project management for global or multi-regional site activation activities.
• Lead start-up delivery (pre-award through activation) and lifecycle maintenance in line 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.
• 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 for 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.
• Mentor team members and contribute to continuous improvement.
• Build strong client relationships and support customer-facing activities.

Required profile

• Bachelor's degree in Life Sciences or a related field.
• Minimum 7 years' experience in clinical research, including 3+ years in a leadership role.
• Proven international project experience across multiple regions.
• Demonstrated ability to deliver projects on time, within scope and budget.

Required skills

• Strong leadership and project management skills, managing multiple priorities.
• Excellent communication, negotiation and stakeholder management skills.
• Ability to lead through others and maintain effective cross-functional relationships.
• Strategic thinking, problem solving, regulatory and clinical trial expertise, and quality and compliance focus.

The potential base pay range, when annualized, is EUR 41,600 to EUR 62,400, depending on qualifications, location and schedule. Incentive plans, bonuses and other benefits may also apply.