Qualifications

Minimum 2 years of Clinical Research experienceCurrent, active State of Florida license as a Registered Nurse OR LPNAssociate degree in NursingActive BLS Must have experience consenting and enrolling participants in clinical trialsAbility to perform clinical tasks including assisting physicians and CRN with minor procedures and other study requirements within scope of practiceAbility to acclimate and integrate into various clinical settings as needed per protocolDemonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs

Shift

Monday-Friday 6:45 am - 3:15pm

Clinical Research Nurse Coordinator (LPN OR RN with research experience)

The Clinical Research Nurse Coordinator under limited supervision to plan, coordinate, evaluate and perform the nursing care of participants and collect data for assigned research projectsFollow study specific protocol guidelines, communicates with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and clinical research support staffWorks to advocate for the patient, while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelinesMaintains adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertionReviews all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA, state, federal and institutional regulations with study candidates and/or legal representative; ensures, through patient advocacy and informed consent as an ongoing process, that the rights, safety, and well-being of trial subjects are the most important considerations and should prevail over the interests of science and societyCoordinates the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols

Pay and Benefits

The pay range for this position is $83200.00 - $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 Jan 22, 2025.

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.