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Recruiter's Glossary
Industry
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Medical Writing
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Sub-Investigator
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Site Management
Clinical Trials Terms
Understanding these terms will help you better evaluate candidates and communicate with hiring managers
CRC
Phase III
Source Documentation
IMP
Protocol Deviation
GCP
Double-Blind
Site Initiation
Patient Recruitment
Database Lock
Safety Monitoring
Randomization
PI
Monitoring Visits
Patient Retention
Regulatory Submission
Risk-Based Monitoring
CTMS
Subject Compliance
Study Coordinator
Placebo-Controlled
CRF
Investigator Meeting
IRB
Inclusion Criteria
ICF
Protocol Amendment
Quality Metrics
Protocol Development
Phase I
Pharmacovigilance
Study Budget
Study Timeline
DSMB
Site Management
Sub-Investigator
Clinical Study Report
EDC
Site Selection
Study Feasibility
Site Close-out
Statistical Analysis
Exclusion Criteria
Data Management
Phase II
AE
Medical Writing
Phase IV
SAE
CRA
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