Clinical Research RN - 252716 at Medix™ Chula Vista, CA
Behavioral Health Market Context
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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
Responsibilities
- •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
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