Clinician, Clinical Assessment Technologies
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Job Description
Clinician supporting psychiatric and cognitive assessments, rater training, and eCOA/ePRO activities. Improving clinical-trial data quality at global CRO Worldwide Clinical Trials.
Responsibilities:
- 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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