Clinical Research Coordinator I (Non‑RN) — Oncology Trials

American Oncology Management Company; Cape Coral (FL); On-site; USD 25,000 - 39,000; Full time

Job summary

American Oncology Management Company in Florida is seeking a Clinical Research Coordinator I (non-RN) to oversee the execution and ongoing management of research studies under the Principal Investigator. This role involves basic protocol tasks, regulatory compliance, and entry-level design of studies (phase 4/observational).

The position supports roughly 5 trials open to accrual annually with 2–10 active patients per year, requiring knowledge of informed consent, adverse event handling, data

Qualifications

• High school diploma required; some college preferred.
• Prior research or medical science experience is a plus.
• Familiarity with regulatory requirements and GCP/ICH guidelines.

Responsibilities

• Coordinate care for patients on clinical research protocols per GCP/ICH/FDA.
• Regulatory/data integrity: IRB/IEC, safety reporting, data review.
• Budget/contract understanding related to study protocols.
• Prepare documents for monitoring visits and maintain trial records.
• Communicate effectively with stakeholders across sites.

Skills

MS Office proficiency

EMR experience

EDC familiarity

CTMS familiarity

Communication skills

Time management

Education

High school diploma

Some college

Tools

Electronic Medical Records (EMR) systems

Clinical Trial Data Entry Systems (EDC)

Clinical Trial Management Systems (CTMS)

MS Office Suite (Word, Excel, PowerPoint, Outlook)

Job description

American Oncology Management Company in Florida is seeking a Clinical Research Coordinator I (non-RN) to oversee the execution and ongoing management of research studies under the Principal Investigator. This role involves basic protocol tasks, regulatory compliance, and entry-level design of studies (phase 4/observational).

The position supports roughly 5 trials open to accrual annually with 2–10 active patients per year, requiring knowledge of informed consent, adverse event handling, data