As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.
We are currently seeking Paramedic III to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose first-in-human food effect drug to drug interactions etc.)
This is a full-time office/clinic-based job in Daytona Beach FL.
If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pharmacokinetics of a new drug.
Many are drawn to their profession because of its direct impact on patient care. If this is your case you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants and as you continue to practice your clinical skills and knowledge youll be involved with the latest medical technologies and treatments witnessing their development firsthand. When the drug you worked with gets approved you know youll touch many patients lives around the world.
WHAT YOU WILL DO:
You will utilize your skills knowledge and clinical judgement to provide a high standard of care clinical research.
Other 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
Monitors meals to ensure dietary compliance by research participants
Assist in the preparation of rooms and medical equipment
Maintain a clean safe and efficient working and study environment
Foster respectful relationships with study participants
Accurately record all research data obtained or observed
Provide training of new staff members
Provide training programs to clinical staff
Observe study subjects for general well-being and potential adverse events taking appropriate action as needed
Transcribe source documentation onto case report forms
Assist with 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.
Takes ownership for the quality and standard of own work.
Other duties as assigned
YOU NEED TO BRING
Current certification as a Paramedic in applicable state.
Current CPR Certification.
3-5 years Paramedic experience
1-2 years Clinical Research experience
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.
What do you get
Regular full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical Dental Vision Life STD/LTD (multiple insurance carriers)
401(K)
Paid time off (PTO)
Employee recognition awards
Multiple ERGs (employee resource groups)
Learn more about our EEO & Accommodations request here.