Paramedic I (On-Call)

Fortrea•Daytona Beach, FL

About The Position

Job Overview: Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements. Summary of Responsibilities: Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Preparation and accurate recording of ECGs/Holters. Accurate and timely collection of blood samples via venipuncture. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Laboratory processing of biological specimens as specified by the protocol. Monitors meals to ensure dietary compliance by research participants. Assist with screening procedures as necessary. Assist in the preparation of rooms and medical equipment. Maintain a clean, safe and efficient working and study environment. Assist with QC of source documents. Transcription of data from source documentation to BDC System. 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. Assist with training of new staff members. Maintains a basic understanding of current regulatory requirements. Attends all required meetings, as appropriate. Assist, 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. Takes ownership for the quality and standard of own work. Check in and check out study participants. May perform IV cannulation in study participants. Administer investigational compounds and perform study-related procedures (ECGs, telemetry, venipuncture, etc.). Monitor participant well-being, document adverse events, and respond to emergencies. Assists with project team to complete projects on time where required. Other duties as assigned.

Requirements

Current certification as a Paramedic in applicable state.
Current CPR/ACLS Certification.
English: Speaking/Writing/Reading
0-2 years Paramedic experience.
Phlebotomy experience.

Nice To Haves

Handling of biologically hazardous or radiolabeled material is necessary.
Must be able to see (distinguish colors) and hear to meet, if necessary, the job requirements.
Ability to work in an upright and /or stationary position for 10-12 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.
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.
Varied hours may be required.
The important thing for us is you are comfortable working in an environment that is : Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Changing priorities constantly asking you to prioritize and adapt on the spot.
Teamwork and people skills are essential for the study to run smoothly.
Technology based . We collect our data directly into an electronic environment.

Responsibilities

Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings.
Preparation and accurate recording of ECGs/Holters.
Accurate and timely collection of blood samples via venipuncture.
Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.
Laboratory processing of biological specimens as specified by the protocol.
Monitors meals to ensure dietary compliance by research participants.
Assist with screening procedures as necessary.
Assist in the preparation of rooms and medical equipment.
Maintain a clean, safe and efficient working and study environment.
Assist with QC of source documents.
Transcription of data from source documentation to BDC System.
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.
Assist with training of new staff members.
Maintains a basic understanding of current regulatory requirements.
Attends all required meetings, as appropriate.
Assist, 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.
Takes ownership for the quality and standard of own work.
Check in and check out study participants.
May perform IV cannulation in study participants.
Administer investigational compounds and perform study-related procedures (ECGs, telemetry, venipuncture, etc.).
Monitor participant well-being, document adverse events, and respond to emergencies.
Assists with project team to complete projects on time where required.
Other duties as assigned.