Sr CRA (Level I) - FSP
200510503Z Thermo Fisher Scientific Pte. Ltd. · Peru
Clinical Research
Remote
Not yet analysed
Demand78
Career growth68
Healthcare fit68
Remote potential45
5-year outlook
Experienced oncology CRAs remain in demand and can progress toward Clinical Trial Manager, Local Study Associate Director, or sponsor oversight roles. Compensation is typically competitive, but exact figures are not stated in the posting.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-22
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering only if you already have 3-5 years of independent CRA/monitoring experience, ideally in oncology. It is not an entry route for clinicians without prior trial monitoring experience.
Who should apply
Oncology nurses, physicians, pharmacists, IMGs, or clinical research coordinators with prior CRA/monitoring experience and ICH-GCP familiarity who want a sponsor/CRO-facing clinical research career.
CV angle
Frame your CV around independent site monitoring across study phases, oncology trial experience, ICH-GCP compliance, EC/IRB and regulatory submissions, CTMS updates, site start-up and close-out, patient recruitment, issue escalation, and inspection readiness. Quantify sites monitored, study complexity, and therapeutic areas where possible.
Skills to highlight
- Independent site monitoring
- Oncology clinical trials
- ICH-GCP compliance
- Regulatory and EC/IRB submissions
- CTMS data updates
- Risk Based Quality Management
- Patient recruitment and site performance
- Inspection readiness
Role summary
A senior Clinical Research Associate monitors oncology clinical trial sites, supports study start-up and close-out, ensures ICH-GCP and regulatory compliance, updates CTMS, manages site issues, and acts as the main site contact within a sponsor/CRO study team.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.