About this opportunity
1103 Team Member Services lists this Clinical Research Coordinator RN II opportunity in sebring, Florida. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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. All the benefits and perks you need for you and your family:
Medical
Dental
Vision Insurance
Life Insurance
Disability Insurance
Paid Time Off from Day One
403-B Retirement Plan
4 Weeks 100% Paid Parental Leave
Career Development
Whole Person Well-being Resources
Mental Health Resources and Support
Pet Benefits
Schedule: Full time
Shift: Day (United States of America)
Address: 4200 SUN N LAKE BLVD
City: SEBRING
State: Florida
Postal Code: 33872
Job Description
Delivers safe care and demonstrates regard for the dignity and respect of all participants. Maintains clinical competencies including physical assessment, phlebotomy, and IV insertion. Practices the principles of Universal Precautions and understands HIPAA regulations. 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 Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. Other duties as assigned. Collaborates with study sponsors and assists site monitors during visits. Serves as liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Coordinates the work of support staff, laboratory technicians, and assistants to ensure efficient and high-quality results. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity. Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation. Reviews informed consent documents with study candidates and ensures patient advocacy and safety. Maintains a clean and prepared clinical space, performing set-up and turnover procedures as needed. Participates in internal and external training programs to maintain licensure. Utilizes positive interpersonal communication skills with healthcare team members, patients, investigators, sponsors, and administration. Works flexible hours and is available for research project-related questions
Knowledge, Skills, and Abilities
Ability to perform clinical tasks including assisting physician, ARNP, 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 in accordance with policies and procedures. Ability to work independently in a fast-paced clinical or research environment. Interpersonal communication skills; ability to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances. Detail-oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure. Ability to simultaneously execute and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties. Specialized knowledge of the unique needs of patients undergoing treatment in research trials including device management trials. Ability to be a critical thinker with an analytical approach to problem-solving. Minimum of two to five years leveraging knowledge of human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology. Minimum two to five years understanding and leveraging of standard clinical practices with regard to informed consent, biospecimen collection, and handling Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skill. Demonstrated proficiencies in clinical study coordination across a spectrum of trial acuities. Knowledge of Federal regulations: Food and Drug Administration (FDA), Centers for Disease Control (CDC), Department of Health and Human Services (DHHS). Bilingual (English/Spanish) preferred. Laboratory specimen preparation and handling preferred. Professional writing skills; Grant writing experience preferred. Knowledge of the levels of growth and development and aging for the adult and geriatric patient population preferred for the adult Clinical Research Nurse. Knowledge of the levels of growth, development, and skills of children between the ages of birth through 18 years of age for the pediatric Clinical Research Nurse preferred.
Education
Associate's of Nursing (Required)
Bachelor's of Nursing (Preferred)
Work Experience
2+ of clinical research experience (Required)
Experience in area of specialty, as assigned (Preferred)
Licenses and Certifications
Registered Nurse (RN) (Required)
Basic Life Support - CPR Cert (BLS) (Required)
Advanced Cardiac Life Support Cert (ACLS) (Preferred)
Certified Clinical Research Professional (SOCRA) (CCRP) (Preferred)
Certified Clinical Research Coordinator (CCRC) (Preferred)
Oncology Certified Nurse (OCN) (Preferred)
Physical Requirements
Physical Requirements -
Pay Range
Pay Range: $66,248.00 - $105,872.00
Background Screening Requirement (Florida Law)
Certain positions are subject to Florida Level 2 background screening, including fingerprinting, as required by state law. Applicants may review general information about Florida’s background screening requirements at the Florida Care Provider Background Screening Clearinghouse:
This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.
Every day, our fellow team members show up to work, unified by one shared mission: Extending the Healing Ministry of Jesus Christ. As a faith-based health care organization, our story is one of hope as we strive to heal and restore the body, mind and spirit. Though our facilities are spread across the country, this unwavering belief binds us together. Across every office, exam and patient room, we’re committed to providing individualized, holistic care. This is our Christian mission, and it inspires us to help make communities healthier and happier.
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Worksite address
sebring, FL, 33876, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.