Clinical Research Assistant, PRN (Registered Nurse)

Care Access•Mobile, AL

3d•Onsite

About The Position

Care Access is dedicated to making the future of health better for everyone by bringing world-class research and health services directly to communities. Through initiatives like the Future of Medicine program, Care Access aims to make advanced health screenings and research opportunities accessible globally. This role is part of a mission-driven team that advances healthcare access by bringing clinical research directly into local communities, offering flexibility in schedule and location. This event-based role allows individuals to support participant care and clinical research event operations. Responsibilities include phlebotomy, specimen handling, documentation, and assisting with the setup and management of research events to ensure they run smoothly, safely, and compliantly. It is a flexible, purpose-driven role where individuals can opt into local events and work as much or as little as desired. The role involves performing venipuncture, handling biospecimens, documenting procedures, maintaining regulatory compliance, managing participant experience, and providing administrative support.

Requirements

Minimum of 1 year performing phlebotomy and specimen handling activities.
Active, unrestricted RN license in the state of practice.
Active and unrestricted State Board of Nursing license in good standing.
Proficiency in venipuncture and specimen handling best practices, with strong attention to labeling, documentation, and chain-of-custody integrity.
Clear, compassionate communication skills and professionalism when engaging with participants and community partners.
Comfort using mobile apps and e-source tools for real-time logging and documentation.
Reliable, punctual, and team-oriented — able to thrive in dynamic event environments and work independently under event-day guidance.

Nice To Haves

Motivated by bringing clinical research to local communities and expanding access to the future of medicine.

Responsibilities

Support participant care and event operations, including phlebotomy, specimen handling, and documentation (paper or electronic).
Help set up and manage clinical research events to ensure they run smoothly, safely, and compliantly.
Perform venipuncture and capillary collections while maintaining aseptic technique and participant comfort.
Handle and prepare biospecimens with care — labeling, processing, packaging, and transferring or shipping under proper chain-of-custody and temperature controls.
Communicate clearly and promptly escalate any safety or quality concerns to onsite leadership.
Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Follow established SOPs to help keep each event audit-ready and compliant.
Welcome participants and help guide them through event flow.
Set up and break down event stations, prepare kits and supplies, and maintain a safe, organized, and professional workspace.
Assist with light administrative and inventory tasks that keep the event running smoothly, from restocking supplies to supporting team coordination.