Paramedic

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.

• Completes training assigned by Client and/or Parexel FSP, as necessary, including general training requirements, SOPs, system, and process related training.
• Adheres to Parexel FSP 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 require

CRS - Paramedic

Primary Duties:

• Owns, maintains, and ensures clinical training transcripts are always up to date.
• 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 Parexel FSP as necessary, including general training requirements, SOPs, system, and process related training.
• Adheres to Parexel FSP and Client SOPs and processes.

Skills and Education:

• Associate in Science degree in Life, Biomedical, or Social science is preferred. Bachelor of Science in a health-related field is desirable.
• Minimum of 1-2 years of work experience in clinical research trials as data collector or clinical coordinator is preferred.
• State of Connecticut licensure as Emergency Medical Technician-Paramedic (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.