Oncology Clinical Research RN - Duly Health and Care

Oncology Clinical Research RN - Lisle - Oncology

Position Highlights:

• Full-Time, 40 Hours/Week
  
• Hours: Monday-Friday; 8:30-5:00pm
  
• Location: Lisle
  

Benefits: 

• Comprehensive medical, dental, and vision benefits that include healthcare navigation assistance and medical coverage at 100% (after deductible) when utilizing a Duly provider.
• Employer provided life and disability insurance.
• $5,250 Tuition Reimbursement per year. 
• Immediate 401(k) match.
• 40 hours paid volunteer time off. 
• A culture committed to Diversity, Equity, and Inclusion (DEI) and Social Impact.
• Up to 12 weeks parental leave at 100% pay and a financial benefit for adoption and surrogacy for non-physician team members once eligibility requirements are met.

The Clinical Research Registered Nurse (RN) will play a key role in the execution of clinical research studies, providing nursing care to study participants while ensuring compliance with study protocols, regulatory requirements, and patient safety. The RN will collaborate with clinical research coordinators, investigators, and other team members to ensure high-quality and timely research outcomes. 

MAJOR RESPONSIBILITIES 

Patient Recruitment and Screening:
o    Assist in the recruitment of potential study participants, including reviewing patient eligibility criteria and conducting screening procedures.
o    Educate and inform patients about study objectives, procedures, and potential risks, ensuring informed consent is obtained.

Study Implementation and Monitoring:
o    Administer study-related interventions, including medications, treatments, and procedures in accordance with study protocols.
o    Perform baseline and follow-up assessments of participants, such as vital signs, lab work, and physical exams.
o    Monitor patient responses to treatment, documenting any adverse events or deviations from the protocol.

Data Collection and Documentation:
o    Collect and record clinical data, ensuring accuracy, completeness, and compliance with protocol.
o    Assist with the preparation of study-related documentation, including case report forms, informed consent forms, and regulatory paperwork.
o    Maintain accurate and up-to-date patient records in the electronic medical record (EMR) system and study databases.

Regulatory Compliance and Safety:
o    Ensure all activities are conducted in compliance with institutional policies, regulatory requirements (e.g., FDA, NCI, IRB), and ethical guidelines.
o    Administer medications and treatments according to protocol guidelines while ensuring patient safety.
o    Identify and report any adverse events or serious adverse events to the appropriate regulatory authorities, investigators, and sponsors in a timely manner.

Collaboration and Communication:
o    Collaborate with the clinical research team, including principal investigators, study coordinators, and other healthcare providers, to ensure study milestones and objectives are met.
o    Participate in study team meetings and contribute to problem-solving related to participant care and study processes.
o    Communicate with patients to ensure their understanding of the study and provide support throughout their participation.

Clinical Research Education and Training:
o    Stay up to date on the latest research, clinical trials, and advancements in nursing practices related to clinical research.
o    Assist in training and mentoring junior nursing staff or research coordinators on study protocols, best practices, and regulatory requirements.

Secondary Responsibilities:
•    Performs other related duties as required. Completes special projects as assigned by the cancer center physicians. 
•    Works independently while maintaining adaptability and flexibility for change.
•    Actively participates in nursing education and committees as assigned.
•    Assists with the orientation of new nursing staff.
•    Attends all mandatory education programs, also specified number of CME seminars, maintains current RN license and certification in CPR.

MINIMUM EDUCATION AND EXPERIENCE REQUIRED
•    Associate’s or Bachelor’s Degree in Nursing from an accredited institution.
•    CPR Certified
•    Three years of related experience required.
•    Clinical Research Coordinator (CRC) certification or Clinical Research Associate (CRA) certification is a plus

MINIMUM KNOWLEDGE, SKILLS, AND ABILITIES (KSA) 
•    Knowledge of oncology nursing.
•    Knowledge of clinical protocols.
•    Ability to communicate effectively, both orally and in writing.
•    Ability to analyze and synthesize data.
•    Ability to maintain patient confidentiality.
•    Knowledge of computer data management systems

The compensation for this role includes a base pay range of $35.28-44.11, with the actual pay determined by factors such as skills, experience, education, certifications, geographic location, and internal equity. Additional compensation may be available through shift differentials, bonuses, and other incentives. Base pay is only a portion of the total rewards package.