RN - Clinical Oncology Research Coordinator- 40 hours- days

Davita Inc.; Detroit (MI); On-site; USD 65,000 - 85,000; Full time

Job summary

A leading oncology research organization seeks an experienced RN to oversee clinical trials and investigational chemotherapy treatment. This position requires coordination across departments, thorough patient education, and adherence to strict guidelines. Ideal candidates will have a valid Michigan RN license and relevant oncology experience.

Qualifications

• Minimum two years of progressive oncology research experience preferred.
• Ability to utilize software for data management essential.
• OCN certification required within three years of hire.

Responsibilities

• Perform assessments and coordinate oncology clinical trials.
• Educate patients on investigational chemotherapy and clinical trial processes.
• Triage patient needs and ensure compliance with clinical protocols.

Skills

Oncology research

Patient education

Coordination of care

Education

Current valid Michigan RN license

OCN certification

ACRP or SOCRA certification

Tools

Computer software

Job description

GENERAL SUMMARY:

Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met and in compliance with IRB and sponsor guidelines. Identify and recruit patients into oncology clinical trials. Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Coordinate patient care across multiple departments/ disciplines, ensuring that the treatment adheres to both strict protocol timelines and the critical clinical timeline that is based on the specific patient scenario/diagnosis. Responsible for providing education regarding diagnosis, clinical trial, and investigational chemotherapy to patients and their families. Responsible for nursing oversight of the investigational chemotherapy treatment. Ensure that chemotherapy orders are written according to the dosing guidelines defined by the clinical trial. Responsible for checking the safety parameters and initiating treatment when patients present for chemotherapy. Triage all patient clinical needs, including immediate and delayed reactions from the investigational agent, which often requires coordination with the patient's primary care physician and external institutions. Initiate direct admissions to the hospital, and referrals to Behavioral Health, Homecare and/or Hospice as appropriate. Support physician investigators and other clinicians as necessary to facilitate patient participation and compliance in oncology. Provide educational in-services on investigational chemotherapy and clinical trial compliance measures to infusion nurses, inpatient staff and other departments as necessary.

EDUCATION/EXPERIENCE REQUIRED:

• Current valid Michigan RN license required.


• OCN certification required within three (3) years of hire into the position. ACRP or SOCRA certification preferred.


• Two (2) years of progressive oncology research experience preferred.


• Ability to utilize computer software to access and input data.

Additional Information

• Organization: Henry Ford Medical Group


• Department: Cancer Clinical & Trans Resear


• Shift: Day Job


• Union Code: Not Applicable