Clinical Research Associate

4 weeks ago


Orlando, Florida, United States ELIXIA LLC Full time
Job Title: Clinical Research Coordinator

At Elixia LLC, we are seeking a highly skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in planning, directing, and coordinating clinical research projects.

Key Responsibilities:

  • Conduct study subject visits, including screening and recruiting subjects, dosing and administering study drugs, and collecting and shipping specimens.
  • Enter patient and research data into designated systems and maintain accurate records of study activity.
  • Monitor study activities to ensure compliance with study protocols and regulatory requirements.
  • Assess eligibility of potential subjects and oversee subject enrollment to ensure informed consent is properly obtained.
  • Record adverse events and side effect data and confer with Investigators regarding reporting to oversight agencies.
  • Prepare for or participate in quality assurance audits and create source documents as assigned.
  • Collaborate with Investigators and Company Management to prepare presentations or reports of clinical study procedures, results, and conclusions.

Requirements:

  • Knowledge of medical terminology and understanding of the principles of administration and management.
  • High School Diploma or degree in nursing or health-related field, with 1-5 years of on-the-job training as a clinical research assistant or research study coordinator.

Continuing Education:

  • IATA (dangerous goods handling) certification.
  • GCP (good clinical practice) certification.
  • BLS/Phlebotomist course, if required for the position.
  • CPR course, as arranged from time to time by the Company on-site.
  • Stericycle Trainings, first week of your start date.

Physical Requirements and/or Environmental Factors:

  • Prolonged periods of sitting at a desk and working on a computer.
  • Prolonged periods of standing and walking around the office.
  • Must be able to lift 20 pounds at times.
  • Travel to sponsor required meetings as needed.
  • Exposure to human bodily fluids.
  • Occasional night and weekend work schedules.
  • Overtime may be required at times.

About Elixia LLC:

Elixia LLC is a leading company in the clinical research industry, dedicated to providing high-quality services to our clients. We are committed to excellence and strive to create a positive and supportive work environment for our employees.



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