Oncology Clinical Research Registered Nurse (RN) - 40 hours/week, day shift
About The Position
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. This position offers a flexible schedule and increased pay rates. The role involves performing and documenting patient and family education regarding protocols, determining patient eligibility for protocol participation, and ensuring all eligibility requirements are met, including informed consent. The nurse will collect and submit protocol study forms, test results, and data accurately and in a timely manner, and fulfill reporting requirements to the Investigation Review Board. Maintaining thorough, accurate, and complete records on all protocol patients, including follow-up queries, dosing modifications, adverse drug reactions, and updates to protocols, is crucial. The position actively participates in protocol review, manages audits of clinical research activities, and is an active member of various committees such as the Oncology Subcommittee, Research group, and cancer committee. The nurse will also participate in tumor boards/conferences to review patients for trial eligibility and communicate with practice RNs for other patients. Additionally, the role assists with the design of protocols, workflows, and policies for research, and communicates with leadership about upcoming trials and patients, educating the team on trials.
Requirements
- 3-5 years of oncology experience
- Superb organizational and communication skills
- Comfortable with autonomous and independent work
- MA RN license
- BLS certification
Nice To Haves
- ONS certification
Responsibilities
- Performs and documents patient and family education regarding protocols including necessary procedures and changes
- Determines patient eligibility for protocol participation
- Ascertains that eligibility requirements have been met, including informed consent to participate in protocol
- Collects and submits all necessary protocol study forms, test results and data accurately and in a timely manner
- Fulfils reporting requirements to the Investigation Review Board
- Maintains thorough accurate and complete records on all protocol patients including follow up queries, dosing modifications with calculations, adverse drug reactions, and update of all protocols upon receipt of amendments, warnings, and other clarifications
- Actively participates in protocol review
- Manages all audits of clinical research activities
- Active member of Oncology Subcommittee, Research group and cancer committee
- Active participant in tumor board/ conference to review patients for trial eligibility and communicates with practice RN for other patients
- Assists with design of protocols, workflows and policies for research
- Communicates with leadership about upcoming trials and patients and educates the team on trials
Benefits
- Flexible schedule
- Increased pay rates
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
