Clinical Research Associate Level II
Thermo Fisher Scientific · Sofia, Bulgaria · Global
Clinical Research
–
Not yet analysed
Demand76
Career growth72
Healthcare fit78
Remote potential45
5-year outlook
CRA roles at large CROs like Thermo Fisher generally offer stable, competitive compensation with a clear ladder toward Senior CRA, CTM, and Clinical Trial Lead positions. Exact figures are not stated in this posting and vary by country and therapeutic area.
Clinical license
Not required
Applicant reach
moderate
Seniority
junior
Employment type
–
Date found
2026-11-05
Intelligence details
Why this is worth applying to
Worth considering if you have some clinical trial exposure or strong GCP grounding and want a structured CRO career ladder — but confirm travel expectations, therapeutic area, and location before investing time. Without a posted description, treat the requirements as unknown until you speak to a recruiter.
Who should apply
Nurses, pharmacists, and doctors with 1-3 years of clinical or research-coordination experience who want to move into CRO-side monitoring; IMGs seeking industry pathways; healthcare graduates with CRC or site-based trial experience.
CV angle
Reframe clinical experience around trial-adjacent evidence: protocol adherence, informed consent discussions, adverse event recognition and documentation, source documentation accuracy, patient safety escalation, and working to SOPs and regulatory standards. Highlight any CRC, audit, data collection, or GCP training even if informal, and quantify site or caseload volume.
Skills to highlight
- ICH-GCP and protocol compliance
- Source data verification and documentation accuracy
- Adverse event and safety reporting
- Site and investigator communication
- Regulatory/SOP adherence
- Clinical data quality and integrity
- Cross-functional stakeholder coordination
- Therapeutic area knowledge
Role summary
A CRA Level II at a large CRO conducts site monitoring visits, verifies trial data against source documents, ensures GCP and protocol compliance, and serves as the main link between sponsor and investigative sites.
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