Clinical trial coordinator
| Highest | $6,000 / mo · United States |
|---|---|
| Experience | 2–4 yrs |
| Degree | Required |
| First paycheck | ~2 to 4 months after bachelor's graduation (via post-study visa) |
Pay in the destination countries
Monthly, in US dollars. Each country is an Imora admission package — open one for that route's fees, language requirement and deadline.
| Country | Monthly |
|---|---|
| United StatesTOEFL 80–100 · $10–70k | $6,000max |
| Hong KongIELTS 6.0–6.5 · HK–200k | $5,700 |
| SingaporeIELTS 6.5 · SGD 18–35k | $5,700 |
| United KingdomIELTS 6.0–7.0 · £11–38k | $5,700 |
| SwitzerlandIELTS 6.5 · CHF 0.9–8k | $5,500 |
| CanadaIELTS 6.0–6.5 · CAD 20–40k | $5,500 |
What does the day look like?
The typical schedule runs Monday through Friday, 08:30 to 17:00 (37.5 to 40 hours per week). Night shifts and heavy on-call duties do not apply, with only rare weekend checks for 24-hour or 48-hour pharmacokinetic blood-draw protocols. Around 45% of the day goes to regulatory and administrative tasks: scheduling patient visits, maintaining the Trial Master File (TMF) and Investigator Site File (ISF), preparing ethics submissions for IRB or IEC review, and tracking investigational medicinal products (IMP) with the pharmacy.
Direct patient interaction takes about 25% of the day: greeting participants, explaining the Patient Information Sheet (PIS), assisting with the Informed Consent Form (ICF), and monitoring for adverse events. Another 20% involves extracting hospital records from Epic Systems or Cerner into EDC platforms like Medidata Rave, Oracle Clinical One, Castor EDC, or REDCap and answering data queries. The remaining 10% is spent hosting CRA monitoring visits.
Where does this lead?
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