Job Description
Job Title: Clinical Research MonitorJob Description
We are seeking a highly skilled Clinical Research Monitor to independently manage monitoring activities and support Phase I and Phase II clinical research studies. The role involves reviewing study documentation, source records, regulatory files, and trial data to ensure protocol compliance and adherence to Good Clinical Practice (GCP).
Responsibilities
+ Conduct independent monitoring activities for clinical trials.
+ Support Phase I and Phase II clinical research studies.
+ Review study documentation, source records, regulatory files, and trial data.
+ Ensure protocol compliance and adherence to GCP.
+ Schedule monitoring visits and prepare monitoring visit reports.
+ Draft confirmation and follow-up letters.
+ Follow up with sites to resolve action items.
+ Resolve Electronic Data Capture (EDC) queries.
Essential Skills
+ 3+ years of cli...
We are seeking a highly skilled Clinical Research Monitor to independently manage monitoring activities and support Phase I and Phase II clinical research studies. The role involves reviewing study documentation, source records, regulatory files, and trial data to ensure protocol compliance and adherence to Good Clinical Practice (GCP).
Responsibilities
+ Conduct independent monitoring activities for clinical trials.
+ Support Phase I and Phase II clinical research studies.
+ Review study documentation, source records, regulatory files, and trial data.
+ Ensure protocol compliance and adherence to GCP.
+ Schedule monitoring visits and prepare monitoring visit reports.
+ Draft confirmation and follow-up letters.
+ Follow up with sites to resolve action items.
+ Resolve Electronic Data Capture (EDC) queries.
Essential Skills
+ 3+ years of cli...