Clinical Research Nurse in Oncology
2 weeks ago
This role is dedicated to providing research coordination for designated oncology studies.
Key Responsibilities:
The responsibilities encompass becoming well-acquainted with study protocols, reviewing medical records, and identifying potential study participants. Duties may include conducting study procedures such as blood draws, preparing specimens for analysis, interpreting lab results, collecting and inputting study data, and maintaining essential documentation.
Clinical Trial Evaluation and Implementation:
Familiarize yourself with study protocols, primary disease categories, and investigational drug information. Ensure effective communication and coordination with various departments involved in the study. Adapt studies in response to amendments and extensions.
Reporting and Financial Documentation:
Complete all necessary reports, including annual study continuation reports required by the Institutional Review Board (IRB). Prepare and submit investigational New Drug (IND) Safety Reports to the IRB.
Medical Management:
Assess the general health of patients, accurately report adverse events within the required timeframe, and notify the Principal Investigator of any changes in patient condition. Assist Principal Investigators in managing adverse events and schedule follow-up procedures as needed.
Study Conduct:
Organize patient visits, laboratory tests, and procedures. Under the guidance of the Principal Investigator, dispense investigational drugs in accordance with protocols and institutional requirements. Collect laboratory samples, obtain vital signs, perform ECGs when necessary, and assist physicians during physical examinations.
Subject Recruitment:
Understand inclusion/exclusion criteria and collaborate with Principal Investigators to prepare recruitment plans. Develop advertisements for institutional approval and liaise with referral sources to screen patients for eligibility.
Documentation and Case Report Form Completion:
Maintain all regulatory documents required by the FDA and sponsors. Ensure accurate documentation and reporting of required procedures/tests and study information. Collaborate with data coordinators to complete case report forms and other data entry promptly.
Additional Duties:
Perform other related tasks as assigned.
Qualifications:
A Bachelor’s degree in Nursing from an accredited institution and a valid Registered Nurse license in the state of Georgia, with a minimum of three years of clinical experience in a specialized field. Alternatively, an Associate's degree in Nursing with at least six years of clinical experience in a specialized area is acceptable. Current American Heart Association Healthcare Provider BLS/BCLS certification is required.
Skills and Abilities:
Strong attention to detail, organizational skills, and proficiency in Microsoft Office and other relevant software/databases are essential.
Work Schedule:
The position requires availability during weekdays, with the possibility of working outside standard business hours.
Compensation and Benefits:
Salary will be commensurate with the qualifications of the selected candidate within the established range. A variety of benefits may be available, including health and dental insurance, retirement plans, and paid time off.
Conditions of Employment:
Candidates must successfully pass a background check prior to employment. All employees are responsible for maintaining the confidentiality and integrity of sensitive information.
Equal Employment Opportunity:
This position contributes to fostering a customer-friendly environment and delivering exceptional service to patients, students, faculty, and staff.
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