CRA - Telemetry Monitor Technician; Part-Time

Duration

12 months contract

• Open 24/7, 100% onsite.
• The training schedule is 4 weeks, M‑F 7a‑3:30p.
• The new position would be pm weekdays and available weekends after completing training. Training would need to occur on 1st shift.
• Final shift:
  Weekdays PM shift 3:00 PM –11:00 PM and Weekends both 3:00 PM –11:00 PM and 11 PM to 7:00 AM overnight shift available (flexible for any shift on weekends).
• For initial training (approx. 4 weeks) it will be a guaranteed 40hr a week. The first 2‑3 weeks will be primarily day shift (7a‑3:30pm). The last week is a combination of PM shift and nights (not 100% in stone, but depending on contractor progress).
• Once training is completed, there are no guaranteed hours. Contractors will be scheduled based on a combination of our needs and their availability. Given how busy we have been and how busy we’ll continue to be, I would estimate a contractor easily receiving 2‑3 shift a week minimum, again based on the above. An example of no hours would be end of the year holidays because there are no subjects in house for 1‑2 weeks.
• 4 weeks training in day shift, Last week will be in 2nd shift training.

• Clinical Pharmacology & Pharmacometrics Research Unit. This role requires face to face interactions with our subjects. It also requires hands on skills that require physical contact with some activities (ex: phlebotomy, ECG collections, vital signs).

• Review protocols and comply with study-specific activities that impact telemetry areas of responsibility.
• Communicates in an appropriate and professional manner with study subjects and unit personnel.
• Maintain accurate and complete source data.
• Perform study protocol related activities, i.e., telemetry monitoring, etc., as assigned.
• Assist with telemetry monitoring system set‑up and preparation of telemetry transmitters and related documentation.
• Participate in continuous cardiac telemetry monitoring of study subjects, as required by the study protocols, and seek assistance as needed.
• Assist with telemetry data review in the telemetry monitoring system and generation of Holter reports, as appropriate.
• Maintain safety and confidentiality of study subjects throughout the study.
• Understands and complies with SOPs, FDA regulations, and basic GCP requirements.

• Cardiac Arrhythmia and phlebotomy.
• Lab work.
• Drawing blood.
• Taking Vital signs.
• Clinical and/or hospital setting. Paramedic and firefighters do well in this position.

• High School Diploma or equivalent.
• 1‑2 years of work experience in a clinical or research environment; and
• Documented proficiency in Cardiac Arrhythmia (must have experience) recognition.

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