Clinical Project Leader, Specialty Solutions

Clario; United States; Remote; USD 28,000 - 40,000; Full time

Benefits offered by this job

Competitive compensation

Remote working

Home office allowance

OTP Szép Card

Engaging employee programs

Job summary

Clario, part of Thermo Fisher Scientific, seeks a Clinical Project Manager to lead clinical trial projects from start-up to close-out in Budapest, Hungary. You’ll drive improvements in study delivery, quality and safety while coordinating sponsors, sites and cross-functional teams.

Responsibilities include managing timelines, resources and budgets, ensuring regulatory and SOP compliance, and mentoring project teams. Some travel up to 20% is required and remote work options are available.

Qualifications

• Bachelor's degree in life sciences or related field.
• Experience leading clinical projects or trial management.
• GCP/ICH knowledge and FDA regulations.
• Strong communication and organizational skills.

Responsibilities

• Lead clinical trial projects from start-up through close-out, managing timelines, milestones, resources and deliverables.
• Identify process improvements to strengthen study quality and safety.
• Collaborate with sponsors, sites and cross-functional teams to translate study requirements into plans.
• Monitor performance, risks and obstacles to ensure high quality delivery.
• Manage project financials including billing, forecasting and pass-through costs.
• Ensure compliance with protocols, SOPs and quality requirements; coordinate with QA.
• Lead and train teams, fostering collaboration and continuous improvement.
• Contribute to client meetings and business development activities as needed.

Skills

Leadership

Communication

Organizational skills

Problem solving

Education

Bachelor's degree in life sciences or related field

Tools

MS Word

Excel

Access

MS Project

Job description

Clario, part of Thermo Fisher Scientific, seeks a Clinical Project Manager to lead clinical trial projects from start-up to close-out in Budapest, Hungary. You’ll drive improvements in study delivery, quality and safety while coordinating sponsors, sites and cross-functional teams.

Responsibilities include managing timelines, resources and budgets, ensuring regulatory and SOP compliance, and mentoring project teams. Some travel up to 20% is required and remote work options are available.