Clinical Research Staff - RN or Paramedic

Paramedic: Owns, maintains, and ensures clinical training transcripts are up to date at all times. Maintains proficiency in various clinical procedures required in study execution. Ensures clinical research studies are conducted according to protocol requirements and internal SOPs, guidelines, work instructions, and process maps. Provides basic first aid and medical/nursing care within scope of practice. Assists in sample management, collection, and generation of computer labels. Records adverse events with referral to medical or nursing personnel for evaluation & treatment. Performs electronic and diagnostic measurements including audiograms, electrocardiograms, visual exams, and other novel devices. Performs and records physical measurements including vital signs and body measurements. Creates volunteer identification (photos, badges). Provides necessary instructions to research participants. Monitors and maintains usage of daily clinic supplies. Maintains equipment log & calibration records. Creates and ensures quality in work and data output by performing data cache review. Attends various clinical meetings (i.e. study start-up, in-service, department meetings, etc.). Supports other additional clinical functions. Demonstrates holistic understanding of work processes at the Unit. Identifies with overall goals of the NHCRU and progresses clinical research studies as planned. Assists in the overall planning and delivery of clinical trials. Assists in the delivery of improved training program. Leads/supervises clinic pCROs (and colleagues, as appropriate) during various shifts of operation as required. Provides/ supervises clinic support activities such as scheduling (e.g., bed space, volunteer, staffing), supply requisitions and training, as required. Collaborates with clinical coordinators and clinical floor leads to maximize study implementation. RN: Owns, maintains, and ensures clinical training transcripts are up to date at all times. Maintains proficiency in various clinical procedures required in study execution. Ensures clinical research studies are conducted according to protocol requirements and internal SOPs, guidelines, work instructions, and process maps. Provides basic first aid and medical/nursing care within scope of practice. Assists in sample management, collection, and generation of computer labels. Records adverse events with referral to medical or nursing personnel for evaluation & treatment. Performs electronic and diagnostic measurements including audiograms, electrocardiograms, visual exams, and other novel devices. Performs and records physical measurements including vital signs and body measurements. Creates volunteer identification (photos, badges). Provides necessary instructions to research participants. Monitors and maintains usage of daily clinic supplies. Maintains equipment log & calibration records. Creates and ensures quality in work and data output by performing data cache review. Attends various clinical meetings (i.e. study start-up, in-service, department meetings, etc.). Supports other additional clinical functions as delegated by the Client. Demonstrates holistic understanding of work processes at the Unit. Identifies with overall goals of the Client’s CRU and progresses clinical research studies as planned. Assists in the overall planning and delivery of clinical trials. Assists in the delivery of improved training program. Leads/supervises clinic contractors (and colleagues, as appropriate) during various shifts of operation as required. Provides/ supervises clinic support activities such as scheduling (e.g., bed space, volunteer, staffing), supply requisitions and training, as required. Collaborates with clinical coordinators and clinical floor leads to maximize study implementation. Completes training assigned by Client and/or PXL, as necessary, including general training requirements, SOPs, system, and process related training. Adheres to PXL and Client SOPs and processes.