Senior Clinical Research Associate
Behavioral Health Market Context
Apply Nowvia Learn4Good
Job Description
ble quality and on-time execution of clinical trials.
• Identify potential sites for participation in clinical trials.
• Perform protocol/site feasibility and Pre-Study Visits to recommend qualified sites.
• Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions as needed.
• Provide feedback to study manuals, Case Report Form completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools, as needed.
• Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in compliance with the approved protocol and monitoring plan.
Requirements
• Bachelor’s degree in a life science or related field of study
• Minimum of 3 – 5+ years monitoring experience
• Oncology, CNS or Pain Management monitoring experience preferred
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• Identify potential sites for participation in clinical trials.
• Perform protocol/site feasibility and Pre-Study Visits to recommend qualified sites.
• Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions as needed.
• Provide feedback to study manuals, Case Report Form completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools, as needed.
• Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in compliance with the approved protocol and monitoring plan.
Requirements
• Bachelor’s degree in a life science or related field of study
• Minimum of 3 – 5+ years monitoring experience
• Oncology, CNS or Pain Management monitoring experience preferred
#J-18808-Ljbffr
Qualifications
- •Bachelor’s degree in a life science or related field of study
- •Minimum of 3 – 5+ years monitoring experience
Benefits
Responsibilities
- •Interact with personnel from study Sponsors, investigational sites, vendors, and functional groups to enable quality and on-time execution of clinical trials
- •Identify potential sites for participation in clinical trials
- •Perform protocol/site feasibility and Pre-Study Visits to recommend qualified sites
- •Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions as needed
- •Provide feedback to study manuals, Case Report Form completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools, as needed
- •Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in compliance with the approved protocol and monitoring plan
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