C

Clairo

Clinical trial endpoint technologies and management

Manager Clinical Training

Corporate & Technical TrainingConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listedRemote

About the Job

Requirements

  • A graduate degree in Psychology, Social Work, Nursing, or a related field is required.
  • Two or more years of experience administering clinician-rated scales in clinical trials or research settings are required.
  • Basic understanding of Good Clinical Practice (GCP) is required.
  • Strong clinical judgment and the ability to identify and address clinical quality or performance issues are required.
  • Demonstrated leadership and training or facilitation skills are required.
  • Exceptional verbal and written communication skills, including the ability to provide clear, constructive, and professional feedback, are required.
  • Ability to work independently and collaborate effectively with cross-functional teams is required.
  • Strong organizational, problem-solving, and decision-making skills are required.
  • Ability to manage multiple priorities and deliver against established objectives and timelines is required.
  • Fluency in English is required.
  • Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint is required.
  • Ability and willingness to work flexible hours across different time zones is required.

Responsibilities

  • Partner with Clinical Science and Clinician Management teams to develop, coordinate, and maintain clinician training and calibration programs, including training materials, plans, exercises, schedules, and documentation.
  • Assign, track, and document clinician training and calibration activities to ensure completion within required timelines and study onboarding requirements.
  • Monitor clinician performance across studies and clinical scales to ensure clinical quality standards are met, identify performance or training gaps, and support resolution of clinical quality issues.
  • Lead group training sessions, team meetings, calibration activities, and supplemental training as needed.
  • Provide clinical consultation and constructive feedback to clinicians and site raters regarding clinical performance.
  • Partner with Clinical Scientists, Clinician Management, and Directors to prioritize training needs and provide recommendations regarding clinician performance and study resourcing.
  • Develop and implement processes, work instructions, process guidelines, and standard operating procedures related to training, calibration, and clinical quality.
  • Oversee Training & Calibration plan requirements and develop metrics to monitor progress and effectiveness.
  • Manage clinical documentation processes to ensure compliance with Good Clinical Practice requirements.
  • Partner with management to ensure operational activities are delivered accurately, compliantly, and on time.
  • Proactively communicate clinical quality concerns and collaborate with relevant teams to resolve them.
  • Work flexible hours as needed to support teams and activities across different time zones.
  • Perform other duties as assigned.

Desired Qualifications

  • Five or more years of clinical experience diagnosing and/or treating patients with psychiatric disorders, neurocognitive disorders, and/or other study-relevant indications.
  • Experience assessing patients with depression, schizophrenia, Alzheimer's disease, or related neuropsychiatric or neurocognitive disorders.
  • Three or more years of experience developing and delivering clinician training, calibration, coaching, or educational programs.
  • Experience with central nervous system (CNS) clinical trials and clinical outcome assessments.
  • Bilingual or multilingual skills.

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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