FSP Clinical Trial Coordinator I
Thermo Fisher Scientific · Remote, Philippines · Global
Clinical Research
Remote
Not yet analysed
Demand70
Career growth65
Healthcare fit78
Remote potential50
5-year outlook
Entry-level CRO coordinator pay is typically modest but stable, with meaningful upside if you progress into CRA, Clinical Trial Manager, or sponsor-side study leadership roles within 3-5 years. Exact figures vary widely by country and cannot be confirmed from this posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
–
Date found
2026-10-19
Intelligence details
Why this is worth applying to
A credible entry point into clinical research for clinicians who want out of direct patient care, especially as a stepping stone to CRA or trial management. However, with no description available, verify location, travel expectations, and pay before investing time.
Who should apply
Nurses, pharmacists, and allied health professionals with some exposure to trials or research who want a structured entry into CRO work; IMGs and healthcare graduates seeking industry experience; doctors considering a move into clinical research operations rather than medical affairs.
CV angle
Reframe ward/clinic experience as protocol-adjacent operational skill: informed consent discussions, patient screening and eligibility, accurate documentation, adverse event recognition and escalation, and multi-stakeholder coordination. Highlight any audit, data collection, or quality documentation work and name specific systems (EDC, CTMS) if genuinely used. Emphasize ICH-GCP training if completed — do not claim trial coordination experience you do not have.
Skills to highlight
- Informed consent and patient eligibility screening
- Accurate clinical documentation and data entry
- ICH-GCP and protocol compliance awareness
- Multi-stakeholder coordination across clinical teams
- Adverse event recognition and escalation
- Regulatory and site file management
- Attention to detail in audit-ready records
Role summary
An entry-level clinical trial coordination role within Thermo Fisher's FSP model, supporting study sites or sponsor teams with regulatory documentation, patient recruitment support, data entry, and visit scheduling. Sits in clinical research operations rather than patient care.
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