Clinical Research Associate I (CRA I) - Oncology
Lifelancer · United States · US
Clinical Research
Remote
Nurse
Pharmacist
Dentist
Demand82
Career growth80
Healthcare fit84
Remote potential15
Salary band
USD 80k – 105k
5-year outlook
Posted range is $80,000-$105,000 annually. Oncology CRA experience is a durable pathway toward senior CRA, lead CRA, or clinical trial management roles, with pay growth tied to monitoring experience and therapeutic-area expertise.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
full-time
Date found
2026-10-26
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- Nurse, Pharmacist, Dentist
- Rate period
- Annual
Why this was classified this way
- contract
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 applying for oncology clinical research coordinators or clinicians with site-level trial experience who want a CRA pathway. Less suitable for candidates without CRC experience or those unable to manage up to 70% regional travel.
Who should apply
Oncology clinical research coordinators, oncology nurses, pharmacists, doctors, and IMGs with hands-on site trial experience, especially in hematology, solid tumors, or early-phase studies.
CV angle
Frame real site-level oncology trial work: patient recruitment and screening support, ICH-GCP compliance, ethics submissions, CRF completion, query resolution, regulatory documentation, site communication, and sponsor/CRO interactions. Emphasize measurable trial milestones and quality outcomes without overstating monitoring authority.
Skills to highlight
- Oncology clinical trial coordination
- ICH-GCP and regulatory compliance
- Site monitoring and quality oversight
- Patient recruitment and retention
- CRF completion and data query resolution
- Ethics Committee submissions
- CTMS/EMR and site file management
- Investigator and site communication
Role summary
A CRA I monitors oncology and hematology clinical trial sites, supports study start-up through closeout, ensures ICH-GCP compliance, tracks recruitment and data quality, resolves site queries, and helps manage site contracts, budgets, and regulatory submissions.
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