RN Clinical Research Night Shift

AdventHealth • Orlando, FL, USA • 19h ago

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:

Night (United States of America)

Address:

601 E ROLLINS ST

City:

ORLANDO

State:

Florida

Postal Code:

32803

Job Description:

Participates in internal and external training programs, staying current and compliant on knowledge and skills applicable to assigned duties. Oversees IV infusions of insulin and glucose during the glucose clamp procedure, as well as the administration of IV Push medications for other procedures. Manages and oversees the dosing of Investigational Products. Supports and upholds clinical research quality standards by participating in protocol compliance, data accuracy, and adherence to regulatory requirements. Other duties as assigned. Maintains a clean and prepared clinical space, performing set-up and turnover procedures in all clinical areas according to standard practices. Communicates effectively with investigators, scientists, project managers, CRCs, staff, and research participants, serving as a participant advocate by reporting needs, concerns, abnormalities, or adverse events. Utilizes resources cost-effectively, maintaining organized and stocked clinical areas, and communicating material needs to the CRC. Maintains clinical competencies such as phlebotomy and IV insertion, and practices Universal Precautions. Keeps accurate and up-to-date source document records for all participants, completing Case Report Forms in a timely manner and ensuring data collection meets protocol specifications. Conducts clinical research trials by escorting volunteers through study visits, performing clinical tasks, collecting data, and communicating results to the Clinical Research Coordinator (CRC) and investigators. Knowledge, Skills, and Abilities:

General knowledge of endocrine and metabolic disease processes [Required]
Ability to perform clinical tasks such as phlebotomy, peripheral IV line insertion, and assisting physicians and providers with procedures. [Required]
Strong interpersonal skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public. [Required]
Ability to handle multiple tasks, simultaneously, in an organized and timely manner. [Required]
Ability to work independently and as a team under the direction of the Investigator, PM, and Clinical Operations Manager [Required]
Critical-thinking skills [Required]
Computer skills, particularly Microsoft Outlook, Word, Excel, Publisher, PowerPoint; use of internet and other research tools [Preferred]
Knowledge of clinical/translational research and research regulatory environment [Preferred]