Paramedic / Madison WI (On-Site)

What You Will Do

• Utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
• Accurate and timely collection of blood samples via venipuncture.
• Laboratory processing of biological specimens as specified by the protocol.
• Accurately perform blood pressure, pulse, respiratory rate and temperature readings.
• Preparation and accurate recording of ECGs/Holters.
• Maintains a clean, safe and efficient working and study environment.
• Foster respectful relationships with study participants.
• Accurately record all research data obtained or observed.
• Observe study subjects for general well-being and potential adverse events, taking appropriate action as needed.
• Transcribes source documentation onto case report forms.
• Assists with Quality Control (QC) of source documents and case report forms.
• Maintains a basic understanding of current regulatory requirements.
• Attends all required meetings, as appropriate.
• Assists, as necessary, with study procedures.
• Maintains accurate records of all work undertaken.
• Maintains skills to perform all study tasks, as required.
• Maintains constant awareness of participant safety and dignity at all times.
• Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.
• Ensures that client and participant confidentiality is maintained.
• Responds to client and team queries in a timely manner.

Key Responsibilities

• Accurate and timely collection of blood samples via venipuncture.
• Laboratory processing of biological specimens as specified by the protocol.
• Accurately perform blood pressure, pulse, respiratory rate and temperature readings.
• Preparation and accurate recording of ECGs/Holters.
• Maintains a clean, safe and efficient working and study environment.
• Foster respectful relationships with study participants.
• Accurately record all research data obtained or observed.
• Observe study subjects for general well-being and potential adverse events, taking appropriate action as needed.
• Transcribes source documentation onto case report forms.
• Assists with Quality Control (QC) of source documents and case report forms.
• Maintains a basic understanding of current regulatory requirements.
• Attends all required meetings, as appropriate.
• Assists, as necessary, with study procedures.
• Maintains accurate records of all work undertaken.
• Maintains skills to perform all study tasks, as required.
• Maintains constant awareness of participant safety and dignity at all times.
• Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.
• Ensures that client and participant confidentiality is maintained.
• Responds to client and team queries in a timely manner.

Physical Requirements

• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
• Causes occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Variable hours may be required.

Benefits

• Medical
• Dental
• Vision
• Life
• STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG’s (employee resource groups)