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Salary
$14k – $35k per year (Estimated)
Location
Remote/Hybrid (Shanghai, China)
Seniority
Junior · 1+ year exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Clario is a healthcare technology company headquartered in Philadelphia, Pennsylvania, with a history dating back to 1972. The organization provides clinical trial endpoint technology and services, including electronic clinical outcome assessments, medical imaging, cardiac safety monitoring, and respiratory solutions. It operates on a global scale, supporting pharmaceutical and biotechnology firms through all phases of clinical research to generate high-quality evidence for regulatory submissions.

Join Clario, a part of Thermo Fisher Scientific and help drive the successful delivery of cardiac safety solutions that support clinical trials around the world. As a Project Manager within our Cardiac Solutions team, you will lead cross-functional project teams through the execution of global clinical studies, ensuring high-quality delivery, exceptional customer service, and adherence to project timelines and budgets. You will serve as a trusted partner to sponsors and internal stakeholders, helping bring life-changing therapies to patients faster through operational excellence and strong project leadership.

What We Offer

  • Competitive compensation and incentives.

  • Engaging employee events and hybrid work technology support.

What You'll Be Doing

  • 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 operational teams.

  • Develop, maintain, and manage study documentation throughout the project lifecycle.

  • Coordinate the distribution, tracking, reconciliation, and management of study equipment and related materials.

  • Create, review, and distribute study status reports, project metrics, and client communications.

  • Ensure appropriate archival of study data, documentation, and project records in accordance with company and regulatory requirements.

  • Establish, manage, and fulfill customer expectations through proactive communication and stakeholder engagement.

  • Monitor study timelines, milestones, and deliverables to ensure successful project execution.

  • Manage financial aspects of assigned studies, including budget reviews, revenue forecasting, scope change assessments, and invoice reconciliation activities.

  • Identify project risks, develop mitigation strategies, and escalate issues appropriately to support study success.

  • Facilitate collaboration between sponsors, vendors, and internal teams to optimize resources, maximize efficiency, and achieve contractual commitments.

  • Lead internal and external discussions and negotiations to support successful study execution and customer satisfaction.

  • Apply structured problem-solving methodologies to address customer concerns, operational challenges, and project escalations.

  • Maintain issue tracking documentation and ensure timely follow-up and resolution of project-related concerns.

  • Present Cardiac Solutions services and operational workflows during investigator meetings, site initiation meetings, and client presentations as required.

  • Participate in business development meetings and support customer discussions regarding operational processes and service delivery.

  • Assist in onboarding, mentoring, and training new Project Management team members.

  • Contribute to departmental initiatives, process improvements, and special projects as assigned.

What We Look For

  • Bachelor's degree or equivalent combination of education and relevant project management experience.

  • 1 to 4 years of project management experience within pharmaceutical, biotechnology, healthcare, clinical research, life sciences, medical device, or related industries.

  • Understanding of the drug development process and clinical trial environment.

  • Experience supporting cardiac safety studies, clinical technology solutions, eClinical platforms, or related clinical research services is preferred.

  • Strong project planning, organizational, prioritization, and time management skills.

  • Experience coordinating multiple stakeholders, timelines, budgets, and deliverables simultaneously.

  • Knowledge of project financial management concepts, including budgeting, forecasting, invoicing, and scope management.

  • Strong risk management and problem-solving abilities with a proactive approach to issue resolution.

  • Excellent verbal and written communication skills with the ability to communicate effectively in English.

  • Strong interpersonal skills and the ability to build productive relationships with sponsors, sites, vendors, and cross-functional teams.

  • Working knowledge of Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams.

  • Detail-oriented with demonstrated responsiveness to customer inquiries and operational requests.

  • Clario Project Management Certification required as applicable to the line of business.

  • 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.

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