Responsible for performing practical and administrative activities of clinical trials in Clinical Pharmacology, in line with protocol and regulatory requirements.
ResponsibilitiesAccurately perform blood pressure, pulse, weights, respiratory rate, and temperature readings.Prepare and accurately record ECGs/Holters.Collect and process biological samples as specified in the protocol and ensure the proper distribution of those samples.Monitor meals to ensure dietary compliance by research participants.Assist with screening procedures as necessary.Assist in the preparation of rooms and medical equipment.Maintain a clean, safe, and efficient working and study environment.Essential SkillsExperience in phlebotomy.Strong computer skills, particularly in electronic charting.Knowledge of medical terminology.Experience in clinical research.Work Environment
This position is onsite, working in a Phase 1 clinical trial setting. The environment requires strict adherence to safety and cleanliness standards, ensuring an efficient and compliant workspace.
Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Daytona Beach,FL.
Application Deadline
This position is anticipated to close on Feb 12, 2025.
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