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Clairo

Clinical trial endpoint technologies and management

Clinical Project Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in Costa RicaNo salary listed

About the Job

Requirements

  • A bachelor's degree in life sciences, pharmacy, nursing, or a related healthcare field, or equivalent experience.
  • One to three years of clinical trials experience within a contract research organization or pharmaceutical research organization, preferably in project management.
  • Expertise in project planning, financial tracking, and regulatory compliance, including Good Clinical Practice, International Council for Harmonisation guidelines, and U.S. Food and Drug Administration requirements.
  • Proficiency in Microsoft Word, Excel, Access, and Project.
  • Ability to lead, communicate, and collaborate cross-functionally.

Responsibilities

  • Lead study startup activities by reviewing protocol requirements, defining project plans, and coordinating documentation with stakeholders.
  • Manage project execution through resource planning, financial oversight, and adherence to standard operating procedures and regulatory guidelines.
  • Provide team leadership by setting performance expectations, delivering training, and supporting coaching and mentoring efforts.
  • Support business development by contributing to capability presentations and representing the company at professional meetings.
  • Oversee project closeout by coordinating submission activities and ensuring completion of all final deliverables.

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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