Pediatric Clinical Research Coordinator RN Orlando Onsite

adventhealth; Orlando (FL); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Benefits from Day One: Medical, Dental

Paid Time Off from Day One

403-B Retirement Plan

Job summary

AdventHealth is seeking a Clinical Research Associate to coordinate the informed consent process for study participants and screen eligibility for clinical trials in Orlando, FL. The role requires RN licensure and strong HIPAA knowledge, with duties spanning documentation, biospecimen coordination, and participant communication.

The successful candidate will work in a fast-paced clinical research setting, supporting investigators and staff while ensuring compliance and quality across study

Qualifications

• 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 environment and manage multiple tasks.
• Knowledge of HIPAA data protection and patient advocacy.

Responsibilities

• Executes and coordinates the informed consent process for participants in clinical trials and research studies.
• Screens potential research participants to determine eligibility for clinical trials and studies.
• Maintains accurate and complete records of the informed consent process.
• Coordinates biospecimen collection and maintains HIPAA-protected data linking patient information to biospecimens.

Education

Associate's of Nursing

Bachelor's of Nursing

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:

• Benefits from Day One: 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: 601 E Rollins St
• City: Orlando
• State: Florida
• Postal Code: 32803

Job Description:

Executes and coordinates the informed consent process for participants in clinical trials and research studies. Screens potential research participants to determine eligibility for clinical trials and studies. Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants. Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns. Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions. Coordinates or performs biospecimen collection and maintains HIPAA protected database connecting patient information to biospecimens used in research. Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets. Conducts research regarding patient screening and clinical eligibility assessments. Coordinates the care and follow-up of volunteers placed on research studies, trials, and programs. Provides ongoing support and information to participants throughout the duration of studies. Works flexible hours and is available for research project-related questions 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. 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. [Required]
• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required]
• Ability to acclimate and integrate into various clinical settings as needed per protocol [Required]
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. [Required]
• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research [Required]
• Ability to communicate effectively with research participants, investigators, research staff and external partners. [Required]
• Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement. [Required]
• Ability to accept direction and respond to the changing needs of clinical research units [Required]
• Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill [Required]
• Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment [Preferred]
• Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials. [Preferred]
• One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology [Preferred]
• Bilingual (English/Spanish) [Preferred]

Education:

• Associate's of Nursing [Required]
• Bachelor's of Nursing [Preferred]

Field of Study:

• Nursing
• Nursing

Work Experience:

• N/A

Additional Information:

• N/A

Licenses and Certifications:

• Registered Nurse (RN) [Required]
• Basic Life Support -