Research Assistant I

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)
• Nursing Clinical Ladder Program*
• Sign-on Bonus*
• Relocation Bonus*
• Team Based Nursing Model*
• Reimbursement for the NCLEX*

* Nursing or BU specific benefits and perks

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: 8:00am-4:30pm

The role you'll contribute:

The Clinical Research Assistant I (RA I) 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 I 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:

           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.

           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

           The RA I will assist the CRC/CRN by communicating patient events and concerns regarding the patient's level of understanding to the CRC/CRN.  Functions as a patient advocate by escalating patient concerns to the CRC/CRN.

           Assists the CRC/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 meet protocol specifications and requirements.

           Has a basic understanding of protocol documents and performs required activities with the assistance of the CRC/CRN.  Communicates with the CRC/CRN incoming data and patient status such as adverse events and inconsistencies. 

The expertise and experiences you'll need to succeed:

          Ability to perform clinical tasks including assisting physician, ARNP, PA, CRC and CRN with minor procedures and other study requirements, as needed.

          Ability to work as a team. under the direction of the CRC, Investigator, Supervisor and Clinical Operations Manager.

          Good communication and time management skills

          Flexible and self-motivated

          Ability to follow responsibilities to completion

          Basic computer skills.

EDUCATION AND EXPERIENCE REQUIRED:

          High school diploma or equivalent