Phlebotomist-SUB-013

Software Galaxy Systems, LLC

Miramar, FL

JOB DETAILS
JOB TYPE
Full-time, Employee
SKILLS
Analysis Skills, Asepsis, Assays, Biology, Calibration, Cleanroom, Clinical Support, Corrective Action, Current Good Manufacturing Practice (cGMP), Documentation, Drug Development, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), Housekeeping/Cleaning, Instrumentation, Interpersonal Skills, Laboratory Techniques, Laboratory Testing, Manufacturing, Microbiology, Product Documentation, Quality Control, Root Cause Analysis, Specimen Collection, Team Player, Test Data, Time Management, Trend Analysis, Writing Skills
LOCATION
Miramar, FL
POSTED
15 days ago

Location: 3340 Enterprise Way Miramar FL USA 33025

Description:
Training Schedule: Training is up to 3 months. This is usually 3 days a week onsite from 6:30am – 3:00pm. Once they complete training, the working hours will fluctuate from 0 hours a week up to 40 hours a week. The associates fill out a form listing the days and hours they can work and the client will schedule as needed. The client cannot guarantee the days and number of hours they might work. Many of the workers have more then 1 job and they are able to fit Teva into their working schedules.

Shift Schedule:
 

Candidates must have open availability to work 1st, 2nd and 3rd shift as scheduled. Shift schedules are given to workers a week in advance.
Typical work schedule is 75%

1st shift and about 25% 2nd shift. 1st – Monday - Sunday 6:30AM to 3:00PM
2nd – Monday - Sunday 2:30PM to 11:00PM
3rd – Monday - Sunday 10:30PM to 7:00AM

Temp to perm: Yes, based on performance and openings
Core essential skill sets to be considered for the role:
1.Must have a current CPR Cardiopulmonary Resuscitation card 2. Experience as a Medical Assistant or phlebotomist

Screening Requirements:
1. Basic Background Check
2. Drug 11 Panel with Fentanyl
3. Medical Screenings:
A) Vision Screen - Near, Far, Color, Depth and Peripheral
B) Vital Signs

Job Summary:
The role of the Research Technician is to serve as an integral member of the site and study team during study processes, including pre-admit, admission, orientation, conduct,
discharge and study close.

Essential Functions:
∙ Performs conduct procedures in strict compliance to the study protocol, Good Clinical Practice standards, Standard Operating Procedures (SOP's), QA/QC procedures, OSHА guidelines and other state and local regulations as applicable
∙ Provides assistance in the execution of clinical trials
∙ Ensures the well-being and safety of study participants
∙ Provides administrative and operational support

Qualifications:
∙ Education A high school diploma or G.E.D. and Phlebotomist certification is required.

Experiencе
∙ One to two (1-2) years of experience in a clinical environment
∙ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
∙ Certification/Licensure N/A
∙ Knowledge, Skills, Abilities (Other pertinent qualifications/skills/knowledge necessary to perform the essential functions of the job)
∙ Able to obtain vital signs and perform ECGs
∙ Able to perform telemetry and insertion of intravenous catheters, or a willingness to learn
∙ Excellent oral, written and interpersonal communication skills
∙ Able to work independently and handle multiple competing priorities
∙ Able to work with tight deadlines
∙ Able to function independently within a team environment
∙ Excellent organizational and time-management skills and a strong attention to detail

∙ Proficient in MS Office Suite (Word, Excel, Outlook)

About the Company

S

Software Galaxy Systems, LLC