Contract Assignment: March 2025 through November 2025
Job Summary:
The Pharmacist is the lead 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.
- Responsible for QA work as delegated.
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:
- Pharmacist with active NYS license.
- At least two years’ experience in clinical nursing or pharmacist role required.
Physical Requirements:
- Prolonged periods of sitting at a desk and working on a computer.
- Must be able to lift up to 15 pounds.
Wage/Salary: $55-65/hour