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Monitoring a clinical trial site

Checking that a trial site follows the protocol, protects participants and keeps complete, accurate records.

Good work shows: Checks consent and eligibility for each participant; records deviations with the date and action taken; follows up open issues before the next visit.

Monitoring a clinical trial site is one of the healthcare skills on FinderK.

The job simulations and Skill Paths below include work that is checked for this skill. You do the work in an original fictional company and get feedback on it.

Job simulations

The trial review before the monitoring visit

Clinical research coordinator at Hallam Road Clinical Research Unit

About 80 minutes. Included in Plus.

Fourteen trial participants to check before the monitor arrives. Find the visit and eligibility deviations, report a major one honestly while the investigator and a nurse push for a softer version, then beat the 24 hour clock on a serious adverse event without making a medical call.

Skills: Check participants against a protocol; Report a deviation honestly and on time; Protect source records under pressure; Meet a safety reporting deadline; Stay inside delegated authority

Skill Paths

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