Clinician, Clinical Assessment Technologies

🔥 18 hours ago

🇺🇸 United States – Remote

💵 $71.5k - $142.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead the clinical aspects of assigned Clinical Assessment Technologies projects • Develop clinical assessments, training content, data review plans, schedules, and timelines • Review study-specific assessment and rater data to support subject eligibility and identify data quality or scoring issues • Coordinate clarification and reconciliation with study sites • Develop clinical training and qualification content for psychiatric and/or cognitive assessments, study protocols, and clinical outcome measures • Conduct patient interviews, remote scoring, and assessments; establish scoring rationale and ranges • Support synchronization of external Clinical Experts • Support eCOA/ePRO activities, including specification review, User Acceptance Testing, assessment-measure research, and scale acquisition and licensing • Partner with study teams, sponsors, sites, investigators, and content experts on study design, assessment quality, and training execution • Analyze assessment review activity and communicate findings through tracking, reports, presentations, white papers, and scientific content • Deliver training to Worldwide staff and investigators • Ensure clinical materials and deliverables meet quality and consistency standards • Contribute clinical expertise to protocol and CRF reviews, research initiatives, data quality discussions, and innovative assessment and training approaches

🎯 Requirements

• Master’s degree, M.D., Ph.D., PsyD, or Pharm.D. in a healthcare-related field plus at least one year of clinical experience administering psychiatric and/or cognitive scales; OR a Bachelor’s degree in a healthcare-related field or RN qualification plus at least three years of such clinical experience • At least five years of experience in clinical trial sites, CROs, rater training organizations, biotech-related industries, or similar environments • Knowledge of operational aspects of Phase I-IV clinical research • Experience with clinical assessments and outcomes, including Clinician and Patient Reported Outcomes, patient interviews, assessment measures, rater training methodologies, and placebo-response mitigation techniques • Ability to develop and manage training plans, data review plans, project schedules, standardized processes, and databases • Analytical skills to work confidently with clinical data and numbers • Familiarity with eCOA/ePRO solutions, training video development, actigraphy, and other innovative assessment technologies • Strong communication and relationship-building skills • Excellent organization and judgment; ability to prioritize responsibilities, solve problems, and manage timelines and budgets • Proficiency in English with excellent written and verbal communication skills • Proficiency in Microsoft Office applications • Advanced Microsoft Excel skills

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Equal employment opportunities • Transparent compensation and pay equity

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