Rn Or Lvn To Administer Vaccines

Job Overview

Coordinate and execute all activities related to the Investigational Product (IP). Participate in clinical research studies ensuring that clinical trial tasks are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.

Essential Functions

• Assists research site with coverage planning related to staffing and scheduling for research projects
• Participates in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standards
• Maintains a safe environment in accordance with site policies
• Assists in providing training to new investigator site staff members on study-specific topics and requirements
• Maintains source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principles
• Complete all required sponsor training
• Preparation and administration of IP to clinical research patients
• Corresponds with research subjects to troubleshoot study-related questions or concerns
• Participates in study process reviews and enhancement efforts to support control of site unit budget, development of the research facilities and site services and the culture towards a high performing research study team
• Updates and maintains site staff skills, training and knowledge of current best nursing practices and topics related to clinical research
• Follow and maintain all blinding procedures with study volunteers and blinded team members
• Assists the investigators to safeguard the well-being of subjects and maintain standards required of clinical research sites
• Actively involved in study data quality checking and query resolution
• Provides clinical research support to investigators to prepare for and execute all tasks related to the investigational product
• Adheres to standard operating procedures (SOPs) and other directives throughout this process
• Maintain responsibility for the management of inventory/IP accountability: i.e., orders, replacements, return of IP study materials
• Reports any deviations from normal research practices to senior staff and implement agreed changes in the study care program
• Reviews study protocols and study documents and instructions related to the investigational product
• Prepares for and attend study monitoring visits, study audits and regulatory inspections with clinical research regulatory agencies
• Assists investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standards
• Record and maintain appropriate temperature of the IP per study protocol
• Ensure appropriate receipts of all investigational product
• Provides guidance and supervision to lower-level site staff to help provide that processes are carried out in line with protocols and SOP's, where applicable

Qualifications

• 2+ years’ experience administering vaccines to patients
• Excellent patient care experience
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
• Proficient in the use of technology.
• Sound knowledge of medical terminology.
• Prior clinical research experience a plus, but not required
• Current, clean nursing license in applicable state
• Ability to maintain confidentiality.
• 2+ years nursing experience

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

Colorado/California/Washington state Pay Transparency : The salary range for this role is $83,600 - $104,500.The actual salary will vary based on factors like candidate qualifications and competencies. Certain roles are eligible for annual bonus, sales incentives and/or stock. Benefits may include healthcare, retirement, paid time off, and more.