Research Rn Jobs

About The Position

Requirements

• Associate’s degree in Nursing.
• RN license in the state where practicing.
• Two years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Excellent organizational and time-management skills.
• Strong written and verbal communication skills.
• Ability to interact professionally with patients, study staff, and external stakeholders.
• Working knowledge of GCP and regulatory requirements.
• Proficiency in Microsoft Office Suite and clinical trial management software.

Nice To Haves

• Bachelor’s degree in Nursing.
• Experience working in an oncology setting.

Responsibilities

• Communicate regularly with study sponsors, CROs, staff, and other stakeholders about questions, concerns, and protocol status.
• Monitor the day-to-day conduct of assigned studies according to protocol requirements, standard operating procedures, and Good Clinical Practice.
• Create or review forms for assigned trials to ensure protocol compliance.
• Maintain study files using standardized document-labeling and filing procedures.
• Implement initial protocols and amendments, and train staff involved in patient treatment and management.
• Maintain an up-to-date contact list.
• Assist with patient screening and eligibility determination.
• Facilitate the informed consent process and ensure consent is appropriately completed.
• Prepare and manage source documents according to standard operating procedures.
• Identify protocol deviations and work with leadership and staff on corrective actions to prevent deviations.
• Assist the data coordinator team with case report form completion and query resolution.
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
• Perform protocol-specific closeout activities with the data coordinator.
• Document all deviations, whether related to a protocol or a standard operating procedure.
• Ensure team members understand and adhere to assigned protocols.
• Perform telephone triage assessments of patients on trial when necessary.
• Educate patients about clinical-trial participation, chemotherapy, biotherapy, investigational-agent administration, and potential side effects.

Benefits

• Medical, dental, and vision insurance.
• 401(k) plan with employer matching.
• Life and disability insurance.
• Health savings and flexible spending accounts.
• Paid time off.
• Flexible schedule.
• Remote-work choices.
• Competitive compensation depending on experience.