Clinical Pharmacist - Data Analytics (Full-Time/Hybrid, 8-Hour Day Shifts)

Tasks

• Attend protocol and sponsor meetings
• Compound medications
• Coordinate investigational drug services
• Dispense prescribed drugs
• Evaluate drug dosages and concentrations
• Identify drug incompatibilities
• Interpret prescriptions
• Liaise between study team and sponsor
• Maintain patient medication records
• Manage drug stability and solubility
• Monitor and prevent chemical reactions
• Participate in audits by regulatory agencies
• Prepare written reports
• Support IRB approved clinical trials

Perks/Benefits

• N/A

Skills/Tech-stack

Audit Support | Clinical trial | Clinical trial support | Drug Compounding | Drug Incompatibility | Drug Stability | Drug Storage | Drug dispensing | Drug formulation | IRB compliance | Medical terminology | Pharmacokinetics | Pharmacology | Prescription review | Protocol evaluation | Regulatory Compliance | Solubility | Trial support