Clinical Research Assistant, Nurse

What We Do Care Access is a unique, multi-specialty network of research sites which operates as one connected team of physician investigators, nurse coordinators, and operations managers. Our goal is to engage every healthcare professional in clinical research and to make clinical trials a care option for every patient. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.
Who We Are We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.
Position OverviewThe Clinical Research Assistant, Nurse is an entry level research position.  This position is responsible for handling Investigational Products (IP) in accordance with study protocols, Good Clinical Practices (GCP), and all other applicable guidelines and regulations including Company Standard Operating Procedures.  The Clinical Research Assistant, Nurse will work closely with the Clinical Research Coordinator to complete participant visits.    What You'll Be Working OnDuties include but not limited to:
Patient Coordination·       Prescreen study candidates  ·       Obtain informed consent per Care Access Research SOP . ·       Complete visit procedures in accordance with protocol. ·       Collect, process and ship specimens as directed by protocol, under the direction of the CRC- Schedule visits with participants, contact with reminders    

Conducts delegated clinical tasks (Nurse specific) and monitoring of research participants in accordance with Good Clinical Practices (GCP), ensuring protocol and regulatory compliance. 
Clinical Tasks Include: ·       Receive and properly store investigational products according to the study manual, study protocol, and/or instructions for use.  ·       Prepare pharmaceutical medications for administration including re-packaging and labeling, according to protocol requirements.  ·       Maintain medication and product inventory records including receipt, dispensing, labeling, accountability, and reconciliation of all study products.  ·       Maintain the blinding of all study products, where applicable·       Maintain all safety standards within the Investigational Product room ·       Maintain dispensing records in accordance with regulations and sponsor requirements.·       Maintain proper storage and security conditions for all medications and investigational products.·       Maintain records of equipment logs in accordance with SOPs; and clean and maintain all equipment and work areas, including sterilization as required.
Documentation·        Record data legibly and enter in real time on paper or e-source documents  ·        Request study participant payments ·       Update all applicable internal trackers and online recruitment systems ·       Assist with query resolution   ·       Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.   ·       Assist with maintaining all site logs  ·       Assist with inventory and ordering equipment and supplies  
Patient Recruitment·        Participate in recruitment and pre-screening events (may be at another location)·        Identify potential participants by reviewing medical records, study charts and subject database     ·        Assist with preparation of outreach materials. ·        Assist with recruitment of new participants by conducting phone screenings   ·        Request medical records of potential and current research participants   ·        Actively work with recruitment team in calling and recruiting subjects  
Other Responsibilities- Interact in a positive, professi