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LPN Clinical Research Assistant Night

Job in Orlando, Orange County, Florida, 32885, USA
Listing for: AdventHealth Orlando Support
Full Time position
Listed on 2026-06-05
Job specializations:
  • Nursing
    Healthcare Nursing, RN Nurse
Salary/Wage Range or Industry Benchmark: 20.38 - 32.6 USD Hourly USD 20.38 32.60 HOUR
Job Description & How to Apply Below

Our promise to you:

Joining Advent Health 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. Advent Health 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-Weekend (United States of America)

Address: 601 E ROLLINS ST

City: ORLANDO

State: Florida

Postal Code: 32803

Job Description

Monitors and reports any deviations from the study protocol or adverse events to the principal investigator. Maintains organized and up-to-date documentation and records for all study activities. Participates in team meetings and training sessions to stay informed about study updates and best practices. Assists in the preparation of study materials, Other duties as assigned. Coordinates and schedules study visits and follow-ups with participants.

Ensures compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Collaborates with investigators, research nurses, and other team members to ensure smooth study operations. Assists in the recruitment, screening, and enrollment of study participants according to protocol criteria. Collects and processes biological samples, including blood draws and other specimen collections. Administers study medications and monitors participants for adverse reactions.

Records and maintains accurate and detailed data in case report forms and electronic databases. Communicates effectively with study participants, providing clear instructions and answering questions.

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, providers, or the CRN 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]
  • Computer skills, particularly Microsoft Outlook, Word, Excel, Publisher, PowerPoint, EMR, use of internet and other research tools [Preferred]
  • Knowledge of clinical/translational research and research regulatory environment [Preferred]
Education

N/A

Field of Study

Graduate of a school of practical nursing

Work Experience
  • 1+ clinical experience [Required]
  • Experience in the clinical/translational research environment [Preferred]
Licenses and Certifications
  • Licensed Practical Nurse (LPN) [Required]
  • Basic Life Support - CPR Cert (BLS) [Required]
  • Advanced Cardiac Life Support Cert (ACLS) [Preferred]
Physical Requirements

Physical Requirements -

Pay Range: $20.38 - $32.60

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.

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