Infusion Nurse - PRN/Contract

M3USA • Tucson, AZ

2h • Onsite

About The Position

M3 Wake Research is an integrated network of premier investigational sites, one of the largest independent, multi-site clinical research companies in the US, conducting over 7,000 successful clinical trials since 1984. M3 USA, established in 2000, provides digital solutions across healthcare, life sciences, and pharmaceuticals, aiming for a healthier world and efficient healthcare systems through trusted digital platforms that engage physician communities. The Infusion Nurse position is an onsite, PRN role in Tucson, AZ. This role involves performing critical trial-related procedures and making important trial-related decisions under the direction of the Principal Investigator. The Infusion Nurse is engaged in Investigational Product handling, including dispensing, dosing, administration, and inventory management. Key responsibilities include collecting information from study participants according to protocols, protecting their health, safety, and welfare, and potentially acting as a study coordinator for limited trials. The nurse will also provide patient consultations and education in an outpatient setting.

Requirements

• Graduate of an accredited school of nursing and accredited Registered Nurse Program
• Current Registered Nurse (RN) Licensure in the state of hire or Current Licensed Practical Nurse (LPN) in the state of hire
• Current Registered Nurse certification in specialty area (if applicable)
• Current provider card in Basic Life Support (BLS), Advanced Cardiac Life Support (ACLS) and Pediatric Advanced Life Support (PALS)
• Minimum of 1 to 2 years of experience performing Infusions

Responsibilities

• Performs activities related to Investigational product such as, but not limited to: handling and preparing, administration, and inventory management.
• Provides patient consultations and education in an outpatient setting under the direction of the physician in charge of the clinical trial.
• Reviews and adheres to assigned research study protocol.
• Maintains proper documentation and completes source documents in a timely manner.
• Ensures that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Collaborates with multidisciplinary team members and Sponsor/CRO/Vendor associates.
• Communicates with the participant as well as the participant’s partner/informant/caregiver.
• Attend and successfully complete all training programs; participate in ongoing conference calls, webinars, and other professional development opportunities.
• Complete provided training and Good Clinical Practice (GCP) training as required.

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level
• Education Level: Associate degree
• Number of Employees: 1-10 employees