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Clinical Team Lead (Oncology)
Flourishresearch · 📍 Denver | Colorado | United States · 🕒 vor 2 Tagen
📊 Lead
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Research Assistant
Auf einen Blick
Research Assistant für Flourish Research Clinical Trial Site gesucht. Onsite Position in Chicago mit Fokus auf Patient Support, Protocol Compliance und Clinical Research Activities.
💰 $20–25/h
📊 Entry-Level
🕒 Vollzeit
🌍 Vor Ort
🗺️ Americas
- Protocol Understanding Ability
- Patient Communication Skills
- Attention to Detail
- Confidentiality Awareness
Clinical Research
Informed Consent
Angegeben: $20–25/h · Marktschätzung: ~$20–26/h.
✅ Geeignet für
- Entry-Level Clinical Trial Professionals
- Healthcare Workers transitioning to Research
- Patient Care-Focused Professionals
🚫 Weniger geeignet
- Remote-Only Seekers
- Candidates ohne Patient Interaction Interest
- High-Stress Sales-Focused Personalities
💡 Gut zu wissen
- Onsite Monday-Friday 40 Hours/Week in Chicago
- Reports zu Team Lead oder CRC
- Non-Exempt (Hourly) Classification
- Protocol Training erforderlich nach Hire
Über das Unternehmen
Flourish Research ist eines der progressivsten klinischen Trial Organisationen mit Stärken in Cardiologie, Metabolic Disorders, Renal, Oncology, CNS und Vaccine Research.
Deine Aufgaben
- Read und Understand Protocols zur Unterstützung von Protocol-Specified Patient Visits
- Clearly und Concisely Dokumentiere Patient Assessments, Observations, Test Results
- Obtain Patient Informed Consent nach Federal Regulations, GCPs und IRB Requirements
- Assist in Creative und Diligent Recruitment von Qualified Study Subjects
- Assist in Scheduling und Conducting Patient Visits according zu Protocol Requirements
- Maintain Accurate und Complete Written Source Documentation von Patient Visits
- Accurately Complete Case Report Forms (CRFs) und Worksheets
- Maintain Confidentiality von Patient und Protocol-Informationen
- Promptly Report Adverse Events zu Team Lead oder Supervisor
- Assist in Accountability von Clinical Trial Materials
- Maintain Ongoing Communication mit Team Lead, CRCs, Site Director
Deine Voraussetzungen
- Completion von Required Training für Clinical Trial Protocol Compliance
- Ability to Read und Understand Medical Protocols
- Strong Patient Communication Skills
- Meticulous Attention to Detail in Documentation
- Ability to Follow Strict Confidentiality Guidelines
- Organizational Skills und Time Management
- Collaborative Mindset mit Team orientation
- Enthusiasm für Clinical Research
Benefits
- Excellent Comprehensive Benefits Package
- Supportive und Collaborative Work Environment
- Endless Growth Opportunities
- Competitive Compensation