LPN Vaccine Coordinator - 5 month contract at Atlas Clinical Research – Rochester, New York
Atlas Clinical Research
Rochester, New York, 14603, United States
Posted on
Updated on
Salary:$28.00 - $30.00/hrJob Function:Admin/Clerical/Secretarial
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About This Position
5 month contract position; full-time hours
Job Summary:
The LPN Vaccine Injector works on all assigned trials and is responsible for understanding and implementing protocols.
Duties/Responsibilities:
Understands and implements the protocol with oversight by the Principal Investigator (MD)
Follows the research protocol directly
Adheres to good clinical practices
Responsible for ongoing, active communication of study progress, questions, issues with Investigator and sub-investigator.
Conducts informed consent and other study procedures for trials as deemed appropriate when not in conflict with unblinded role.
Understands the drug preparation instructions and storage directions for the study drug to be administered.
Ensures study drug is dispensed, prepared, administered and returned per assigned protocols as unblinded injector
Documents and tracks the drug accountability for vaccines per study and any required logs
Completes study source documents as required by the study
Receives and logs in drug as arrived, creates tracking logs for accountability as needed
Works with study sponsor and unblinded monitor as directed.
Required Skills/Abilities:
Excellent verbal and written communication skills.
Excellent interpersonal and customer service skills.
Excellent organizational skills and attention to detail.
Strong clinical background with evidence of independent relevant clinical assessment skills preferred.
Education and Experience:
LPN or RN with active NYS license.
At least two years’ experience in clinical role required.
Job Summary:
The LPN Vaccine Injector works on all assigned trials and is responsible for understanding and implementing protocols.
Duties/Responsibilities:
Understands and implements the protocol with oversight by the Principal Investigator (MD)
Follows the research protocol directly
Adheres to good clinical practices
Responsible for ongoing, active communication of study progress, questions, issues with Investigator and sub-investigator.
Conducts informed consent and other study procedures for trials as deemed appropriate when not in conflict with unblinded role.
Understands the drug preparation instructions and storage directions for the study drug to be administered.
Ensures study drug is dispensed, prepared, administered and returned per assigned protocols as unblinded injector
Documents and tracks the drug accountability for vaccines per study and any required logs
Completes study source documents as required by the study
Receives and logs in drug as arrived, creates tracking logs for accountability as needed
Works with study sponsor and unblinded monitor as directed.
Required Skills/Abilities:
Excellent verbal and written communication skills.
Excellent interpersonal and customer service skills.
Excellent organizational skills and attention to detail.
Strong clinical background with evidence of independent relevant clinical assessment skills preferred.
Education and Experience:
LPN or RN with active NYS license.
At least two years’ experience in clinical role required.
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Job Location
Rochester, New York, 14603, United States
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