Job Description

Key Responsibilities

• Administer study medications as prescribed and perform clinical procedures including phlebotomy, blood draws, and vital sign monitoring in accordance with study protocols.
• Initiate peripheral IV lines without the use of tourniquets, following protocol-specific guidelines.
• Conduct thorough reviews of participants’ current medications and accurately document findings in source documentation.
• Administer concomitant medications as required.
• Support daily clinical operations to ensure efficient workflow and high-quality care for research participants.
• Complete and maintain study source documentation, including cMAR, fluid balance logs, adverse events (AE), and concomitant medication records.
• Monitor and document participant responses to treatment, including identifying and reporting adverse events (AE/SAE), and completing required intake forms.
• Identify and resolve discrepancies within study documentation.
• Maintain adequate inventory of clinical supplies and consumables.
• Assist with onboarding and training of new staff, including skills assessment and protocol education.
• Provide oversight and guidance to Research Assistants and technical staff on nursing-related study procedures, including specimen collection and handling.
• Support compliance-related processes in partnership with Human Resources, including exposure incident documentation and follow-up.
• Maintain employee health records, including immunizations (e.g., TB, Hepatitis B).
• Develop study-specific reference materials and summaries for nursing and research staff.
• Participate in ongoing training and education for clinical staff related to study protocols and procedures.

Required Qualifications

• Bachelor of Science in Nursing (BSN)
• Experience in critical care, acute care, or clinical research
• Active BLS and ACLS certifications
• Ability to work 12-hour overnight shifts

Preferred Qualifications

• Prior clinical research experience
• Flexibility with scheduling, including openness to partial/half shifts

Schedule

• 3 days per week, with some weekend availability required
• Overnight shifts: 6:00 PM – 6:00 AM

Highlights

• Flexible scheduling options, including potential for half shifts
• Opportunity to work in a dynamic clinical research environment with hands-on patient care

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