Health Plan Nurse Coordinator I
Behavioral Health Market Context
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Benefits
Pay and benefitsPay Range: $42.00/hourly - $52.00/hourlyPay is based upon candidate experience and qualifications, as well as market and business considerationsERA Health Research provides eligible employees with an opportunity to enroll in a comprehensive benefits package which includes:Medical, dental, and vision insuranceFlexible Spending Account (FSA) and Health Savings Account (HSA) options401k Retirement Savings PlanPaid time off (PTO) starting at10 days per year and 1 hour of sick leave for every 40 hours worked2 Floating Holidays per year6 more items(s)
Qualifications
- •A valid and current Registered Nurse (RN) license in Texas is a mandatory requirement for this position
- •Applications without a Texas RN license will not be considered
- •Current Registered Nurse (RN) license in the applicable state
- •1 year of Nurse experience
- •Basic understanding of medical terminology
- •Strong attention to detail and organizational skills
- •Ability to follow detailed instructions and protocols
- •Good written and verbal communication skills
- •Proficient with basic computer software (MS Office)
- •~ Experience in Clinical research or a relevant clinical setting
- •7 more items(s)
Responsibilities
- •This role is an entry-level role focused on learning the fundamental principles of clinical research coordination under close supervision
- •This individual supports the research team by performing routine data collection and administrative tasks, ensuring compliance with protocols and regulatory standards
- •Assist with patient screening and recruitment for clinical trials
- •Support the informed consent process under the direct supervision of a senior CRC or manager
- •Perform basic clinical data entry and management into Electronic Data Capture (EDC) systems
- •Assist with scheduling patient visits and procedures
- •Help with the preparation of source documents and study binders
- •Maintain inventory of study supplies and equipment
- •Handle processing and shipment of lab samples following IATA/DOT regulations (with training)
- •Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific)
- •Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.)
- •Administer investigational products (drugs, devices, biologics) per protocol
- •Monitor patient responses to investigational products and provide clinical care
- •Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor
- •Provide patient education and serve as a clinical resource for participants throughout the study
- •In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager
- •These additional duties will fall within the scope of the role and contribute to the overall success of the team
- •14 more items(s)
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