Clinical Research Nurse

3 weeks ago

Orlando, United States Actalent Full time

Clinical Research Nurse (TRI)

Job Description

The Clinical Research Coordinator II RN (CRC-II RN) is responsible for planning, coordinating, evaluating, and performing the nursing care of participants and collecting data for assigned research projects. This role requires following study-specific protocol guidelines, communicating with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff. The CRC-II RN advocates 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.

Responsibilities

+ Deliver safe care and demonstrate regard for the dignity and respect of all participants.

+ Maintain skills in clinical competencies including physical assessment, phlebotomy, and IV insertion.

+ Practice the principles of Universal Precautions and understand HIPAA regulations.

+ Maintain a clean, prepared clinical space, and perform set-up and turnover procedures in all clinical areas per SOPs.

+ Participate in internal and/or external training programs to maintain licensure.

+ Utilize positive interpersonal communication skills; communicate effectively 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.

+ Manage multiple clinical trial protocols, coordinate execution and follow-up, utilize resources, and work independently.

+ Perform accurate, legible, and timely documentation; manage records, study medication, and test articles confidentially and securely.

+ Promote PI oversight by advising the PI, sub-investigators, Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to trial integrity and subject safety.

+ 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 trial experience

+ Data collection

+ Oncology

+ Dose calculations

+ Consenting

+ Collecting data

+ Dosing

+ Diabetes management

+ Clinical research

+ GCP knowledge

+ EKG proficiency

+ Registered Nurse

Additional Skills & Qualifications

+ Ability to perform clinical tasks including assisting physicians and CRN 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.

+ Associate degree in Nursing

+ Minimum 2 years of Clinical Research experience

+ Current, active State of Florida license as a Registered Nurse

+ BLS certification

Work Environment

Hospital setting fully onsite.

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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