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 Orlandois 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/Days

Hours: 6:45am-3:15pm *NO WEEKEND/HOLIDAYS

Location: AdventHealth Translational Research Institute

The role you'll contribute: * MUST HAVE PHLEBOTOMY EXPERIENCE

The Research Assistant II (RA II) will assist the Clinical Research Coordinators (CRC)/Research Nurse in the conduct of Phase I-IV industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA Regulations, and ICH/GCP Guidelines. The RA II is immediately accountable to the CRC/CRN and works with them and other study team members to meet study-specific goals and timelines and communicates appropriately and effectively with subjects, investigators, CRC's and other staff. 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:

• Develops methods to assist the CRC/CRN in screening all new patients and consults for trials. Conforms to all standards of good research practice and provide support to research patients by abiding current IRB, FDA, federal, state and institutional regulations pertaining to human subjects research, including the use of institutional and departmental SOP's
• Delivers safe care and demonstrates regard for the dignity and respect of all participants. Practices the principles of Universal Precautions. Understands and abides by HIPAA regulations.
• The RA II will assist the CRC/CRN in coordinating and facilitating study-required activities of trial participants. Assures the consent process has been fully executed. Communicates patient events and concerns regarding the patient's level of understanding to the CRC/CRN. Functions as a patient advocate. Provides support to and is a resource person for questions and information required by patients and families.
• Assists the CRC and CRN in maintaining neat, organized, accurate, and up-to-date source document records for all participants. Completes Case Report Forms (CRF's) or subject tracking tools in a timely manner. Ensures that all data collection and submissions meet protocol specifications and requirements.
• Understands the protocol document and performs required activities as exhibited through collaboration with the CRC/CRN. Communicates with the CRC/CRN incoming data and patient status such as adverse events and inconsistencies.

Qualifications
What You Will Need:

• Graduate of a Medical Assistant, EMT or Paramedic program with previous clinical experience OR
• 3 years clinical experience OR
• 2 years clinical research experience
• BLS
• If MA - American Association of Medical Assistants (AAMA) Certification, or American Medical Technologist (AMT) Certification, or ARMA (American Registry of Medical Assistants), or NCCT (National Center for Competency Testing), or NHA (National Health Career Association)
• If EMT - Current active State of Florida EMT license
• If Paramedic - Current active State of Florida Paramedic license

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