FSP_Clinical Trial Coordinator (Sponsor: Roche)
Thermo Fisher Scientific · Remote, Korea, Republic of · Global
Clinical Research
Remote
Not yet analysed
Demand70
Career growth65
Healthcare fit72
Remote potential50
5-year outlook
Entry-to-mid level CRO compensation, typically modest at the coordinator tier but with a clear ladder into CRA, CTM, and sponsor-side trial management roles where earnings rise meaningfully. Exact figures depend on country, contract type, and FSP terms, which are not stated here.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
–
Date found
2026-10-23
Intelligence details
Why this is worth applying to
Worth considering if you want a low-barrier entry point into industry clinical research with a major CRO and a blue-chip sponsor name on your CV. Confirm the contract type, location policy, and GCP requirements first, since the posting gives no detail.
Who should apply
Nurses and allied health staff with ward or clinic coordination experience, IMGs and healthcare graduates seeking a first industry role, pharmacists familiar with protocols and documentation, and doctors exploring a move away from direct patient care into trial operations.
CV angle
Reframe real clinical experience around trial-adjacent transferables: patient recruitment and consent conversations, accurate documentation and record-keeping, protocol/SOP adherence, multi-stakeholder coordination across departments, audit and inspection readiness, and any exposure to research studies, audits, or data collection. Name specific systems used (EDC, CTMS, hospital EHR) only if genuinely used, and state GCP training status honestly.
Skills to highlight
- Patient recruitment and screening support
- Documentation accuracy and record-keeping
- Protocol and SOP compliance
- Multi-stakeholder coordination
- Data entry and database quality
- Informed consent process awareness
- Audit and inspection readiness
- Clinical terminology and patient pathway knowledge
Role summary
An embedded coordinator role within Thermo Fisher's FSP model, supporting Roche-sponsored clinical trials through site communication, trial document management, data entry and query resolution, recruitment tracking, and general study administration under ICH-GCP.
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