C

Clairo

Clinical trial endpoint technologies and management

Clinical Project Manager - Specialty Solutions

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree or equivalent relevant experience; a background in life sciences, pharmacy, nursing, healthcare, or a related field is advantageous.
  • Previous project or management experience in the clinical development of investigational medicines.
  • At least 1 year of clinical trials experience within a CRO or pharmaceutical research organization, ideally in a project management-related role.
  • Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, FDA regulations, standard operating procedures (SOPs), and clinical trial quality requirements.
  • Ability to identify opportunities for continuous improvement and turn them into practical improvements.
  • Strong organizational and leadership skills.
  • Ability to use Microsoft Word and Excel.
  • Ability to travel up to 20% when required.

Responsibilities

  • Lead clinical trial projects from study start-up through close-out, managing timelines, milestones, resources, and project deliverables.
  • Identify improvements that strengthen study processes, quality, and safety.
  • Partner with sponsors, sites, and cross-functional teams to translate study requirements into practical project plans and solutions.
  • Monitor project performance, anticipate risks, and remove obstacles to support consistent, high-quality delivery.
  • Manage project financials, including billing, forecasting, scope changes, revenue reporting, and pass-through costs.
  • Ensure project teams understand and follow protocols, standard operating procedures, and applicable quality requirements, working with Quality Assurance when deviations or clarifications arise.
  • Lead, train, and support project teams by creating clear expectations and encouraging collaboration and continuous improvement.
  • Contribute project and clinical expertise to client meetings, Investigator Meetings, and Business Development activities as needed.

Desired Qualifications

  • A background in life sciences, pharmacy, nursing, healthcare, or a related field is advantageous.
  • Medical imaging experience is advantageous.
  • Experience using Microsoft Access and Microsoft Project is beneficial.

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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