Research Assistant I Tri

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

-          Benefits from Day One

-          Paid Days Off from Day One

-          Career Development

-          Whole Person Wellbeing Resources

-          Mental Health Resources and Support

-          Pet Insurance*

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: Days

Location: 301 EAST PRINCETON STREET, Orlando, 32804

The community you’ll be caring for: AdventHealth Orlando

• Located on a lush tropical campus, our flagship hospital, 1,368-bed AdventHealth Orlando 

• Serves as the major tertiary facility for much of the Southeast, the Caribbean and South America  

• AdventHealth Orlando houses one of the largest Emergency Departments and largest cardiac catheterization labs in the country 

• We are already one of the busiest hospitals in the nation, providing service excellence to more than 32,000 inpatients and 125,000 outpatients each year 

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: 

• Practices the principles of Universal Precautions and understands and abides by HIPAA regulations.
• Conforms to all standards of good research practice and provides support to research patients by abiding by current IRB, FDA, federal, state, and institutional regulations pertaining to human subjects research.
• Assists the research team by communicating patient events and concerns regarding the patient’s level of understanding.
• Functions as a patient advocate by escalating patient concerns to the research team.
• Assists the research team in maintaining neat, organized, accurate, and up-to-date source document records and databases for all participants.
• Completes Case Report Forms (CRFs), subject tracking tools, registries & databases in a timely manner, ensuring that all data collection meets protocol specifications and requirements.
• Has a basic understanding of protocol documents and performs required activities with the assistance of the research team.
• Communicates with the research team regarding research project status, patient statuses (such as adverse events) and data inconsistencies.
• Assists with source document completion for all required/reported data and submits data within the specified time frame.
• Assists with the maintenance of study charts, registries, and other research documents to coincide with current patient status.
• Maintains a clean, prepared clinical space and performs set-up and turnover procedures in all clinical areas per SOPs and/or Working Instructions in a timely manner.

The expertise and experiences you’ll need to succeed:

• High School Grad or Equiv Required
• 3+ Work Experience Required
• Ability to perform clinical tasks including assisting physician, ARNP, PA, CRC and CRN with minor procedures and other study requirements, as needed.