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Internal Medicine
Job ID:
Requirements:
• Experience:
o Neurology Assessments
o Clinical trial research
o Telehealth
• Certifications:
o Good Clinical Practice (GCP) certification
Scheduling:
• No Call
• Must be available for at least 20 hours a week. Visits can be between 8a-9p
**Willing to License!**
Job Description:
Our providers will be aligned with patients and follow the visit schedule for the trial throughout the patient's journey as part of the study. Calendly will be used as the primary scheduling tool for patients to meet with the physician.
Responsibilities:
• Oversight of Subject Eligibility: Ensure patients meet the criteria for trial participation.
• Review Columbia Suicide Severity Rating Scale (C-SSRS) Assessments: Monitor and evaluate patient safety and mental health.
• Oversight of Adverse Event (AE) Relatedness/Severity Assessments: Assess and manage any adverse events during the trial.
• Decide on Discontinuation of Trial Treatment/Emergency Unblinding Treatment: Make critical decisions regarding patient safety and trial integrity.
• Sign Case Report Forms: Authenticate and approve trial documentation.
• Oversight of Clinical Reports: Review and interpret reports from ECG and central lab testing.
Additional Tasks:
• Conduct and Record Video Neurological Examination Assessments: Submit assessments for Eligibility Review Committee.
• Perform Protocol eCOA Efficacy and Safety Assessments: Oversee assessments such as TETRA S-ADL, CGI-S, C-SSRS, and participant PGI-S, PGI-C.
• Determine Subject Eligibility: Evaluate patient suitability for trial participation.
• Assess Physical Exam Results: Interpret physical exam findings.
• Review Lab Results for Clinical Significance: Analyze laboratory results to determine their impact on patient health and trial outcomes.
• Interpretation of Reports: Analyze and understand clinical reports (ECG, etc.
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