Project Manager, Cardiac Solutions

• Lead the planning, setup, monitoring, and closeout phases of cardiac safety studies and programs.
• Gather customer requirements and translate study needs into actionable plans for cross-functional teams.
• Develop, maintain, and manage study documentation throughout the project lifecycle.
• Coordinate equipment distribution, tracking, reconciliation, and inventory management activities.
• Create, review, and distribute study reports, project metrics, status updates, and customer communications.
• Ensure study data, documentation, and project records are archived in accordance with company and regulatory requirements.
• Establish, communicate, and successfully manage customer expectations throughout project execution.
• Monitor study timelines, deliverables, milestones, and resource utilization to ensure successful outcomes.
• Manage project financial activities, including budget reviews, revenue forecasting, scope management, and invoice reconciliation.
• Identify project risks, develop mitigation plans, and escalate issues appropriately to ensure study success.
• Lead internal and external discussions to support effective communication, teamwork, and efficient use of resources.
• Apply structured problem-solving methodologies to address operational challenges, customer concerns, and project escalations.
• Maintain issue tracking documentation and ensure timely follow-up and resolution of project-related matters.
• Participate in investigator meetings, site initiation meetings, and customer governance discussions as required.
• Present Cardiac Solutions services, workflows, and operational capabilities to customers and stakeholders.
• Collaborate with Business Development and operational teams to support customer engagement and business growth initiatives.
• Assist with onboarding, mentoring, and training new Project Management team members.
• Support continuous improvement initiatives and special projects that enhance quality, customer satisfaction, and operational performance.

What We Look For

• Bachelor's degree and demonstrated project management experience within clinical research, life sciences, healthcare technology, or a related industry.
• Clario Project Management Certification required as applicable to the line of business.
• 1 to 4 years of experience in project management within pharmaceutical, biotechnology, clinical research, healthcare, medical device, or related industries.
• Understanding of the drug development process and clinical trial lifecycle.
• Experience managing customer-facing projects, operational deliverables, timelines, and budgets.
• Strong organizational, planning, prioritization, and time-management skills.
• Excellent verbal and written communication skills, including the ability to communicate effectively in English.
• Strong interpersonal and relationship-building skills with the ability to collaborate effectively across global teams.
• Working knowledge of Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams.
• Detail-oriented with strong analytical and problem-solving abilities.
• Demonstrated responsiveness, accountability, and commitment to customer satisfaction.
• Ability to manage multiple priorities and adapt effectively in a fast-paced environment.
• Valid passport and willingness to travel internationally up to approximately 20% as business needs require.

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.