Job Title: Clinical Research Nurse Coordinator (LPN or RN - Infusion, Contract/Part-Time)
Job Description
This temporary, part-time Clinical Research Nurse Coordinator role offers an excellent opportunity for an experienced LPN with infusion skills to support a clinical research team in a structured research environment. You will work with consented patients enrolled in clinical trials, providing high-quality patient care and infusion services while supporting study-related procedures and documentation.
Responsibilities
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Provide safe and accurate infusion services to patients enrolled in clinical research studies.
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Deliver compassionate, high-quality patient care throughout each clinical visit.
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Support the execution of clinical trial protocols under the direction of the research team.
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Accurately document patient assessments, treatments, and study-related procedures in accordance with clinical research and regulatory requirements.
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Monitor patients during and after infusions, promptly reporting any adverse events or concerns to the appropriate clinical personnel.
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Assist with patient education regarding visit procedures and study-related expectations.
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Collaborate closely with the clinical research team to ensure smooth patient flow and adherence to study schedules.
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Maintain a clean, organized, and compliant clinical environment that supports safe patient care and research activities.
Essential Skills
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Active LPN or RN license in good standing.
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Demonstrated infusion experience in a clinical setting.
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Strong patient care skills with a focus on safety, comfort, and clear communication.
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Proficient documentation skills with attention to accuracy and completeness.
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Ability to follow clinical protocols and detailed procedures reliably.
Additional Skills & Qualifications
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Clinical research experience is a plus but not required.
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Comfort working with patients enrolled in clinical trials.
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Strong organizational skills and the ability to manage multiple tasks in a structured environment.
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Ability to work effectively as part of a multidisciplinary clinical research team.
Work Environment
You will work in a structured clinical research environment caring for consented patients enrolled in clinical trials. The setting emphasizes protocol-driven care, accurate documentation, and close collaboration with a dedicated research team. The role offers a flexible, part-time schedule on a temporary contract basis, providing a balance between professional engagement and personal commitments. You will work in a professional clinical space equipped for infusion services and research procedures, with established processes to support patient safety, regulatory compliance, and high-quality clinical research.
Job Type & Location
This is a Contract position based out of St. Petersburg, FL.
Pay and Benefits
The pay range for this position is $34.00 - $35.00/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 St. Petersburg,FL.
Application Deadline
This position is anticipated to close on May 29, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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