Clinical Research Nurse II

Clinical Research Nurse II

This role focuses on coordinating and implementing oncology clinical research studies and therapeutic treatment protocols in a mission-driven environment dedicated to improving cancer outcomes. The Clinical Research Nurse II recruits, consents, and educates research participants and their families, conducts patient assessments and study visits, administers study-related interventions, and ensures strict adherence to protocol and regulatory requirements. This position offers the opportunity to gain highly valued oncology research experience and to work closely with engaged investigators on impactful cancer trials.

Responsibilities

• Coordinate and implement oncology clinical research studies and therapeutic treatment protocols in accordance with approved protocols and regulatory guidelines.
• Recruit, screen, and consent eligible research participants, ensuring they and their families clearly understand study procedures, risks, and benefits.
• Educate research participants and their families about study requirements, treatment plans, and follow-up expectations to support informed participation.
• Conduct comprehensive patient assessments and perform protocol-required study visits, including baseline and follow-up evaluations.
• Administer study-related medications, treatments, and research interventions as appropriate, following clinical and research standards.
• Monitor participants closely for adverse events and promptly document, report, and escalate safety concerns in line with Good Clinical Practice (GCP) and institutional policies.
• Collaborate with investigators, physicians, research coordinators, and sponsors throughout the study lifecycle to ensure high-quality execution of trials.
• Serve as a clinical resource for patients, families, and research staff, providing guidance on oncology care and study-related procedures.
• Maintain accurate, timely, and complete study documentation, including source documents, case report forms, and regulatory files, to ensure protocol compliance.
• Assist with data collection, data entry, and study-related reporting, supporting the integrity and reliability of clinical trial data.
• Participate in sponsor monitoring visits, audits, and inspections by preparing required documentation and responding to queries.
• Support patient retention and engagement throughout study participation by building trust, addressing concerns, and coordinating follow-up visits.
• Work within current oncology disease teams, with current openings focused on the Myeloma team, to manage assigned patients and studies effectively.

Essential Skills

• Active registered nurse (RN) license in the state of Georgia.
• Minimum of three years of nursing experience.
• Clinical research and clinical trial experience, particularly in oncology settings.
• Demonstrated experience in oncology within current disease teams.
• Proficiency in patient recruitment, screening, and consenting for clinical studies.
• Experience conducting patient visits and assessments in accordance with research protocols.
• Strong skills in adverse event monitoring, documentation, and reporting.
• Working knowledge of Good Clinical Practice (GCP) guidelines and their application in clinical research.
• Ability to collaborate effectively with investigators, physicians, coordinators, sponsors, and multidisciplinary care teams.
• Strong attention to detail and organizational skills to maintain accurate study documentation and ensure protocol compliance.

Additional Skills & Qualifications

• Interest in gaining highly valued oncology research experience in a mission-driven environment focused on improving cancer outcomes.
• Ability to serve as a clinical resource and educator for patients, families, and research staff.
• Strong communication skills to support patient engagement, retention, and understanding of complex oncology treatments and protocols.
• Comfort working with a defined patient volume, typically managing 15-20 active treatment patients per coordinator.
• Adaptability to work within specialized oncology disease teams, including Myeloma.
• Commitment to supporting high-quality clinical trials that contribute to the approval of new oncology therapies.

Work Environment

The role is primarily onsite, providing direct patient care and research support in a clinical research setting. Typical work schedules begin between 7:00 AM and 9:00 AM, offering some flexibility within standard daytime hours. Current openings are on the Myeloma team, with assigned patient volume typically ranging from 15 to 20 active treatment patients per coordinator, allowing for focused and meaningful patient relationships. There is no routine travel between locations required for current openings, enabling stability in the worksite. The environment is mission-driven with strong investigator engagement and support, emphasizing collaboration, high-quality oncology research, and improved cancer outcomes.

Job Type & Location

This is a Contract to Hire position based out of Atlanta, GA.

Pay and Benefits

The pay range for this position is $40.00 - $43.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Nov 10, 2026.

Workplace Type

This is a fully onsite position in Atlanta, GA.