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Clairo

Clinical trial endpoint technologies and management

Lead Project Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeTokyo, JapanHybrid

About the Job

Requirements

  • A bachelor's degree and demonstrated project management expertise within clinical research, life sciences, healthcare technology, or a related industry.
  • 5 to 10 years of experience within pharmaceutical, biotechnology, clinical research, eClinical technology, or related industries, with a strong emphasis on project management.
  • A strong understanding of the drug development process and clinical trial lifecycle.
  • Demonstrated ability to mentor, coach, and develop project management professionals.
  • Strong financial management experience, including budgeting, forecasting, scope management, and revenue tracking.
  • Excellent organizational, prioritization, and time-management skills.
  • Verbal and written communication skills, including the ability to communicate effectively in English.
  • Strong stakeholder management, negotiation, and relationship-building capabilities.
  • Proficiency with Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams.
  • Ability to manage multiple priorities and complex study portfolios simultaneously.
  • Ability to identify risks, solve problems, and drive operational improvements in a fast-paced environment.
  • A valid passport and willingness to travel internationally up to approximately 20% as business needs require.

Responsibilities

  • Manage and develop Project Management team members through coaching, mentoring, performance feedback, and career development activities.
  • Ensure appropriate onboarding, training, and documentation requirements are completed and maintained for assigned staff.
  • Review system configurations, study setups, and project documentation to ensure quality standards and operational requirements are met.
  • Lead routine status meetings to monitor team workload, project performance, resource allocation, and forecasting activities.
  • Monitor performance metrics and support team development through continuous improvement and operational excellence initiatives.
  • Lead study planning, startup, monitoring, execution, and closeout activities for neuroscience eCOA programs and studies.
  • Gather customer requirements and translate study needs into actionable plans for cross-functional operational teams.
  • Develop, maintain, and oversee study documentation, reports, study records, and project deliverables.
  • Manage study timelines, budgets, revenue forecasts, scope changes, invoice reconciliation activities, and financial performance.
  • Establish and maintain sponsor relationships through proactive communication and expectation management.
  • Identify project risks, develop mitigation plans, and escalate issues to ensure successful study outcomes.
  • Lead internal and external negotiations while fostering collaboration, accountability, and effective resource utilization.
  • Develop and implement problem-solving strategies to address customer concerns and resolve escalations in a timely manner.
  • Track, monitor, and communicate project status, deliverables, risks, and financial performance to stakeholders.
  • Present study services at investigator meetings, site initiation meetings, customer governance meetings, and operational reviews.
  • Support business development initiatives by presenting operational capabilities, data workflows, and service offerings to prospective and existing customers.
  • Drive operational readiness for new product initiatives and ensure successful implementation within the Neurosciences line of business.
  • Support process standardization and consistency across studies, programs, therapeutic areas, and customer portfolios.
  • Contribute to departmental strategy, operational objectives, and continuous improvement initiatives.

Desired Qualifications

  • Experience leading customer-facing projects, programs, or portfolios within an eCOA, eClinical, clinical technology, or CRO environment.

About the Company

Clairo

Clinical trial endpoint technologies and management

Clario provides clinical trial endpoint technologies, including software, connected devices, and artificial intelligence to collect and analyze data across cardiac safety, eCOA, medical imaging, precision motion, and respiratory endpoints. Its platform supports site-based, hybrid, and fully decentralized trials, gathering data from devices, questionnaires, and imaging, then processing and analyzing it to produce reliable clinical evidence, with integrated training and 24/7 support. The company differentiates itself with a broad end-to-end suite plus deep regulatory expertise and a global deployment network that enables rapid localization in 100+ languages. Its goal is to simplify the clinical trial process while improving patient safety and retention, promoting patient choice and diversity, and advancing health equity by prioritizing both physical and mental well-being.

Company size
5,001-10,000
Company stage
Acquired
Total funding
$29.9M
Headquarters
London, United Kingdom
Founded
1972

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