Referso Jobs

FSP CRA 2 & Sr. CRA - Oncology

Fortrea · Posted Nov 13, 2026

Open

Remote, United States
Remote
Full-time · Mid
$118K–$145K per year
3+ years

FSP CRA 2 & Sr. CRA - Oncology

Fortrea · Posted Nov 13, 2026

Open

Remote, United States
Remote
Full-time · Mid
$118K–$145K per year
3+ years

FSP CRA 2 & Sr. CRA - Oncology - Northeast & West Coast US

Lifelancer · Posted Nov 15, 2026

Open

Remote, United States
Remote
Full-time
$118K–$145K per year
3+ years

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Senior Clinical Research Associate responsible for monitoring oncology clinical trials across the United States, including site visits, data review, SAE reporting, and project coordination.

Compensation

Target Pay Range: $118-$145K based on title

Responsibilities

Conduct routine monitoring and close-out of clinical sites
Maintain study files and conduct pre-study and initiation visits
Liaise with vendors and manage site operations
Ensure protocol compliance and patient protection
Review CRFs and generate queries

Requirements

University or college degree, or certification in a related allied health profession
Nice to have: ophthalmology experience

Skills

clinical monitoring oncology expertise CRF review data management SAE reporting feasibility work site management

FSP CRA 2 & Sr. CRA - Oncology & Multi Specialty TAs - Remote US

Lifelancer · Posted Nov 12, 2026

Open

Remote, United States
Remote
Full-time
$110K–$118K per year
3+ years

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Responsible for all aspects of study site monitoring, site management, data integrity, SAE reporting, and project coordination for oncology and multi-specialty clinical trials.

Compensation

Target Pay Range: $110-$118K based on title

Responsibilities

Conduct routine monitoring and close-out of clinical sites
Maintain study files and conduct pre-study and initiation visits
Liaise with vendors and ensure protocol compliance
Ensure data integrity of CRFs and other data collection tools
Perform CRF review, query generation and resolution

Requirements

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
Nice to have: Ophthalmology experience

Skills

Clinical Monitoring CRF review Query generation SAE reporting Registry management Feasibility work

In-House Clinical Research Associate II, Sponsor-Dedicated (Contract)

Premier Research · Posted Oct 14, 2026

Open

United States
Contract · Mid
3–5 years

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Support clinical trials for biotech, medtech, and specialty pharma companies as a secondary contact for sites and remote monitor.

Responsibilities

Partner with cross‑functional team members and study sites throughout all phases to support trial elements
Carry out remote monitoring of clinical trials
Serve as the secondary contact for sites supporting CRAs
Report and follow up on SAEs and ensure all reportable events are documented and reported per protocol
Address non‑compliance issues and communicate them clearly

Requirements

Bachelor's degree in a clinical, biological, scientific, or health‑related field or equivalent
Nice to have: Experience in Neurology or Psychiatry
Nice to have: Experience with Schedule I controlled substances

Skills

Clinical trials experience Remote monitoring SAE reporting Non‑compliance management Audit/inspection readiness

SAE reporting jobs

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