Clinical Research Coordinator, Nurse (RN)

US Oncology Network-wide Career Opportunities; England; On-site; GBP 30,000 - 60,000; Full time

Job summary

An exciting opportunity awaits in a leading oncology group, where you will play a crucial role as a Clinical Research Coordinator or RN. This position focuses on supporting innovative cellular therapy trials, ensuring compliance with protocols, and collaborating with healthcare professionals to enhance patient care. You will engage in detailed assessments, manage regulatory documentation, and communicate effectively with both patients and physicians. Join a dedicated team committed to advancing cancer care in a dynamic and supportive work environment, where your contributions will make a significant impact on patient outcomes.

Qualifications

• Experience in clinical research preferred.
• Ability to read and interpret technical procedures.

Responsibilities

• Present trial concepts and conduct assessments for eligibility.
• Collect and maintain regulatory documents as per protocols.
• Collaborate with physicians to review patient conditions.

Skills

Clinical Research

Data Entry

Communication Skills

Regulatory Compliance

Education

Associate's Degree in Clinical or Scientific Discipline

BSN (preferred)

Tools

Database Management

Job description

Overview

Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research Coordinator or Clinical Research RN to support our office in Norfolk.

***Please take this quick survey once you've submitted your resume to complete the application process: Clinical Research PI Link

****If you have completed the survey before, even for another position, please do not take it again.

Responsibilities

• Present trial concepts, objectives, and treatment details to potential patients for various cellular therapy trials, conducting detailed assessments and screenings to determine eligibility.
• Participate in the informed consent process and enroll patients on protocol.
• 80% of the job will be computer-based; direct patient care is limited in a non-RN Clinical Research Coordinator role.
• Collect and maintain regulatory documents in accordance with USOR SOP and applicable regulations. Participate in scheduling monitoring and auditing visits, and interact with monitors/auditors onsite.
• Coordinate patient care in compliance with protocol requirements.
• Collaborate with physicians to review patients for changes in condition, adverse events, medication use, protocol compliance, and response to the drug study; document all findings thoroughly.
• Work directly with other research bases and/or sponsors.
• Oversee the preparation of orders by physicians to ensure protocol compliance.
• Communicate with physicians regarding study requirements, dose modifications, and adverse event reporting.

Qualifications

• Associates degree in a clinical or scientific discipline required.
• Experience in clinical research preferred.
• Experience with computer data entry and database management.
• Excellent written and oral communication skills.
• Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents.

Additional Qualifications for Nurse Candidates

• Graduate from an accredited nursing program (BSN preferred).
• Minimum of one (1) year nursing experience, preferably in oncology.
• Current RN licensure in Virginia preferred.
• Current BCLS or ACLS certification required.
• OCN, SoCRA, or ACRP certification preferred.

Work Environment

The work environment involves exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations, and other conditions common in an oncology/hematology clinic. Employees may have direct contact with patients and potential exposure to hazardous substances, including chemotherapeutic agents.

Physical Demands

Requires full body motion, handling and lifting patients, manual dexterity, and eye-hand coordination. Standing and walking for extended periods are necessary, with occasional lifting of up to 40 lbs. Corrected vision and hearing are required.