Job Description

Job Title: Clinical Research Nurse - Oncology

Job Description

The Clinical Research Coordinator II RN (CRC-II RN) serves under limited supervision to plan, coordinate, evaluate, and perform the nursing care of participants and collect data for assigned research projects. The CRC-II RN adheres to study-specific protocol guidelines, communicates with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff. This role involves advocating for the patient while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. The CRC-II RN delivers safe care, demonstrating regard for the dignity and respect of all participants while maintaining clinical competencies, including physical assessment, phlebotomy, and IV insertion.

Responsibilities

• Deliver safe care and demonstrate regard for the dignity and respect of all participants.
• Maintain skills in clinical competencies such as physical assessment, phlebotomy, and IV insertion.
• Practice the principles of Universal Precautions.
• Understand and abide by HIPAA regulations.
• Maintain a clean and prepared clinical space, performing set-up and turnover procedures in all clinical areas as per SOPs in a timely manner.
• Participate in internal and/or external training programs to maintain licensure.
• Utilize positive interpersonal communication skills, effectively communicating with healthcare team members, patients, investigators, sponsors of research, and administration.
• Review all elements of the current institutional IRB approved informed consent document with study candidates and/or legal representatives.
• Ensure patient advocacy and informed consent as an ongoing process, prioritizing the rights, safety, and well-being of trial subjects.
• Manage multiple clinical trial protocols, coordinate the execution and follow-up of each protocol, and perform accurate, legible, and timely documentation.
• Manage records, study medication, and test articles in a confidential and secure manner.
• Promote PI oversight by advising the PI, sub-investigator(s), Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to the integrity of the trial and/or the safety of research subjects.
• Coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.

Essential Skills

• Clinical research experience in oncology.
• Experience with clinical trials and chart review.
• Ability to pre-screen patients.
• Proficiency in data management and EDC.
• Ability to perform clinical tasks such as assisting physicians and CRNs with minor procedures and other study requirements within scope of practice.
• Ability to acclimate and integrate into various clinical settings as needed per protocol.
• Demonstrated skills in clinical competencies, including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs.

Additional Skills & Qualifications

• Associate degree in Nursing.
• Minimum 2 years of clinical research experience.
• Current, active State of FL license as a Registered Nurse.
• BLS certification.

Work Environment

The position involves working in a hospital setting, ensuring adherence to research protocols and maintaining a clean and prepared clinical space. The role requires the ability to perform set-up and turnover procedures in all clinical areas as per SOPs in a timely manner.

Pay and Benefits

The pay range for this position is $75000.00 - $98000.00

Benefits from Day One

Paid Days Off from Day One

Career Development

Whole Person Wellbeing Resources

Mental Health Resources and Support

Pet Insurance*

Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

Workplace Type

This is a fully onsite position in Orlando,FL.

Application Deadline

This position will be accepting applications until Dec 13, 2024.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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