Clinical Research Staff (CRS) RN (D/E)

Primary Duties CRS- 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.