Clinical Research Staff - RN or Paramedic

External Job Description On site position in New Haven, CT***** Must have CT Licensure and ACLS Responsibilities: 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. Qualifications • Preferred Associate in Science degree in Life, Biomedical, or Social Science. Bachelor of Science in a health-related field desirable. • Preferred qualifications include minimum of 1-2 years of work experience in clinical research trials as data collector or clinical coordinator. • State of Connecticut licensure as EMT-P. • Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures. • Proficiency in Microsoft (MS) Office and the ability to learn different software programs. • Current certification in Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) required. • Ability to work beyond normal work hours and various shift availability required. RN Primary Duties: 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. Skills and Education: • Minimum of an Associate in Science degree in Life, Biomedical, or Social science. Bachelor of Science in a health-related field desirable. • Minimum of 1-2 years of work experience in clinical research trials as data collector, clinical coordinator, or clinical research nurse is preferred. • State of Connecticut licensure as RN. • Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures. • Proficiency in Microsoft (MS) Office and the ability to learn different software programs. • Current certification in Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) required. • Ability to work beyond normal work hours and various shift availability required. #LI-LG4 #LI-REMOTE Apply tot his job