Oncology Clinical Research RN — Full-Time, Mon-Fri

The US Oncology Network; McAllen (TX); Sur place; USD 85 000 - 115 000; Plein temps

Avantages offerts par ce poste

Tuition Reimbursement

Employee Assistance program

Wellness program

Retail discounts

Résumé du poste

Texas Oncology in McAllen, TX seeks a Full-time Senior Registerd Nurse (RN) to support oncology clinical research. The role offers a structured weekday schedule (Mon-Fri, 8:00am-5:00pm) with no weekends, on-call, or major holidays.

The senior RN level will align with experience (Level 1, 2, or Sr) in a leading community oncology setting. Responsibilities include screening for trials, informed consent, adverse event assessment, staff education, and precise trial documentation.

Qualifications

• Graduate from an accredited nursing program.
• Current licensure as a registered nurse in state of practice.
• BLCS or ACLS certification required.
• Minimum 1 year of RN experience.
• OCN certification preferred; CCRP/CCRC preferred.
• Oncology or research experience preferred.

Responsabilités

• Screen potential patients for clinical trial participation with physicians.
• Present trial concepts to oncology patients and obtain informed consent.
• Assess adverse events and condition changes in patients.
• Educate staff and patients on investigational product management.
• Ensure accurate documentation and data entry for trials.
• Serve as liaison between clinic departments for proper trial conduct.

Connaissances

RN licensure

ACLS/BLCS

Oncology experience

Clinical research

Team collaboration

Formation

Nursing degree (BSN preferred)

Description du poste

Texas Oncology in McAllen, TX seeks a Full-time Senior Registerd Nurse (RN) to support oncology clinical research. The role offers a structured weekday schedule (Mon-Fri, 8:00am-5:00pm) with no weekends, on-call, or major holidays.

The senior RN level will align with experience (Level 1, 2, or Sr) in a leading community oncology setting. Responsibilities include screening for trials, informed consent, adverse event assessment, staff education, and precise trial documentation.