All the benefits and perks you need for you and your family:

• Benefits from Day One

• Paid Days Off from Day One

• Student Loan Repayment Program

• 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)

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full-Time / Shift : Day (8a.m. - 4:30p.m.)

Location: 6 601 EAST ALTAMONTE DRIVE, Altamonte Springs, 32701

The role you’ll contribute:

The Clinical Research Coordinator I (RN) i s involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities to include: Research participant recruitment and consenting for the therapeutic areas they serve, provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies, and the coordination of biospecimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance.

Through collaboration with research assistants and/or clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems. Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents. Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.

The value you’ll bring to the team:

• Execute and coordinate the informed consent process for AdventHealth Research Institute participants in clinical trials and research studies across multiple locations.This may require travel between sites and research laboratories, and/or the use of technology.

• Delivers safe care and demonstrates regard for the dignity and respect of all participants.Maintains adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertion.Practices the principles of Universal Precautions.Understands and abides by HIPAA regulations.

• Maintains a clean, prepared clinical space.May perform set-up and turnover procedures in all clinical areas, per SOP’s, in a timely manner.

• Participates in internal and/or external training programs to maintain licensure.

• Responsible for all aspects of research conducted including patient screening, assessing (clinical) eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs.

• Coordinate or perform biospecimen collection (i.e. blood, tissue) and maintain HIPAA protected database connecting patient information to biospecimens used in research; perform patient chart review and data collection.

Qualifications

EDUCATION AND EXPERIENCE REQUIRED:

• Associate degree in Nursing

LICENSURE, CERTIFICATION OR REGISTRATION REQUIRED:

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

• BLS

• Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.

• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner

LICENSURE, CERTIFICATION OR REGISTRATION PREFERRED:

• Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)

• 1-year Research Oncology Experience

• Other certification as applicable to clinical degree or program (i.e. medical assistant, medical technician, phlebotomy)

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location.

Category: Research

Organization: AdventHealth Orlando

Schedule: Full-time

Shift: 1 - Day

Req ID: 24001479

We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.