Clinical Research- RN

The US Oncology Network•Bensalem Township, PA

About The Position

Alliance Cancer Specialists, a member of The US Oncology Network, is seeking a Clinical Research Coordinator, RN, to support and manage clinical trials within our oncology Bensalem and Langhorne practices. This role is responsible for the screening, enrollment, coordination, and ongoing management of patients participating in clinical research studies while ensuring strict compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The ideal candidate is highly organized, detail‑oriented, and comfortable working independently in a fast‑paced clinical environment.

Requirements

Graduate of an accredited nursing program required (BSN preferred)
Current Registered Nurse (RN) license in the state of practice
Current BLS or ACLS certification required
Minimum of 3 years of nursing experience required
Ability to read, analyze, and interpret clinical trial protocols, informed consent documents, and regulatory materials
Strong organizational, time‑management, and multitasking skills
Ability to work independently and prioritize competing responsibilities
Excellent written and verbal communication skills
Strong interpersonal skills with the ability to collaborate across departments
High attention to detail and accuracy
Ability to function effectively in a fast‑paced clinical environment

Nice To Haves

OCN certification strongly preferred
SoCRA or ACRP certification preferred
Oncology experience strongly preferred
Prior clinical research experience preferred

Responsibilities

Screen and identify potential patients for clinical trial eligibility and oversee subject recruitment to meet enrollment goals
Present clinical trial concepts, risks, and benefits to patients and participate in the informed consent process
Coordinate and manage patient care in accordance with study protocols and clinical trial requirements
Perform ongoing patient assessments, including monitoring for adverse events, changes in condition, concomitant medication use, and response to study treatment
Accurately document all study‑related activities and patient data in a timely manner
Dispense investigational drugs, provide patient education regarding administration, and maintain drug accountability records
Review physician orders to ensure protocol compliance and communicate study requirements, dose modifications, and adverse event reporting needs
Conduct billing compliance reviews using protocol‑specific billing guides and submit billing information to appropriate personnel
Maintain regulatory documentation in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOPs), GCP, and applicable federal, state, and local regulations (OSHA, CDC, HIPAA)
Coordinate and participate in monitoring and auditing visits, serving as the onsite liaison for monitors and auditors
Educate clinic staff and patients on clinical research protocols, procedures, and requirements
Collaborate with the Study Research Leader (SRL) in study selection and implementation
Work cross‑functionally with physicians, clinic staff, and research teams to resolve complex issues related to trial participation
Participate in required training and education programs and contribute to continuous improvement of research policies and processes