
51 - 200 employees
Founded 2000
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Clinilabs is a global, full-service Contract Research Organization (CRO) specializing in the development of central nervous system (CNS) drugs, devices, and technology. The company provides comprehensive services to pharmaceutical, biotechnology, and medtech organizations, supporting their projects from first-in-human to Phase 3 clinical trials. Clinilabs is dedicated to addressing the significant unmet needs in CNS drug development, focusing on neurological, mental health, and substance use disorders.
🕒 September 29
🇺🇸 United States – Remote
💵 $35 / hour
⏱ Part Time
🟡 Mid-level
🟠 Senior
⬇️ Data Entry
🦅 H1B Visa Sponsor
👻 Ghost score 15%
Where this job comes from
Posted on Clinilabs's careers page ↗, not through a job board
First seen by Remote Rocketship September 29
Still open on Clinilabs's site. Checked 5 hours ago.

51 - 200 employees
Founded 2000
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Clinilabs is a global, full-service Contract Research Organization (CRO) specializing in the development of central nervous system (CNS) drugs, devices, and technology. The company provides comprehensive services to pharmaceutical, biotechnology, and medtech organizations, supporting their projects from first-in-human to Phase 3 clinical trials. Clinilabs is dedicated to addressing the significant unmet needs in CNS drug development, focusing on neurological, mental health, and substance use disorders.
• Process files according to project-specific criteria and internal standard operating procedures • Process PSG, MSLT, MWT, EEG, or other types of data • Provide complete documentation, reports, and summaries of activity • Meet reliability standards and maintain reliability performance through annual re-certification • Work in a timely manner until assigned work is complete without error • Attend regular data processor review meetings • Score digital data according to currently accepted criteria and systems • Maintain a kappa score of .80 or higher for sleep stage scoring and meet other project-specific quality and reliability metrics • Respond to data queries in a timely manner • Follow and ensure compliance with current Good Clinical Practices (GCPs) • Adhere to corporate policies and procedures • Conduct benchmark studies when assigned by management • Perform other duties as assigned
• At least 5 years of prior scoring experience • Ability to meet and maintain reliability standards of performance • PSG Data Processors require Registered Polysomnographic Technologist (RPSGT) credentials and/or PhD with comparable experience • College degree preferred • Good problem-solving, documentation and communication skills • Ability to apply logic and good clinical judgement related to the data • Flexible and regular availability according to project assignment and schedule • Ability to complete a minimum of 10 files per week • Ability to adhere to a 1 scorer to 1 participant policy, as required by project assignment
• Training is compensated at a rate of $35 per hour
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