Research Technologist

Sonic Healthcare USA•Las Vegas, NV

1d•Onsite

About The Position

We're not just a workplace - we're a Great Place to Work certified employer! Proudly certified as a Great Place to Work, we are dedicated to creating a supportive and inclusive environment. At Sonic Healthcare USA, we emphasize teamwork and innovation. Check out our job openings and advance your career with a company that values its team members! Quality is in our DNA -- is it in yours? You’ve got problem-solving instincts, a passion for patient care, and the drive to keep things running smoothly. You’re also looking for great benefits, the support of an all-star team, and an opportunity to grow your career. Join our front line of #HealthcareHeroes! Our mission is to advance the health and wellbeing of our communities as a leader in clinical laboratory solutions. The Research Technologist will be responsible for assisting the Principal Investigator in operationalizing clinical protocols relevant to Bio-specimen procurement initiatives. Location: Las Vegas, Nevada Hours: 8:00 am - 5:00 pm Days: Monday - Friday Fulltime/Benefit Eligible

Requirements

Pathology Assistant or advanced Med-tech degree and certification preferred.
BA/BS/MA/MS science related degree preferred.
A minimum of 2-5 years’ experience as an Instrument Operator, Laboratory Manager or equivalent in a licensed and certified laboratory setting
Selected individual must possess in depth understanding of Clinical Laboratory Medicine.
Applicant must possess experience working with highly detailed clinical research protocols and be able to understand and put into practice technical procedures necessary to complete research objectives.
Applicant must possess experience in histology
A valid state driver’s license with an acceptable Motor Vehicle Report (MVR)
Must have personal and reliable transportation
Proof of current vehicle registration and personal automobile insurance
Excellent verbal and written communications skills
Experience with patient interaction
Knowledge of basic medical terminology
Ability to understand and abide by Food & Drug Administration: Good Clinical Practice Guidelines
Skilled in interacting effectively with hospital staff, patients and other personnel
Comfortable in a pathology environment

Nice To Haves

Experience or knowledge of cytology, molecular biology and pathology strongly desired.
Prior supervisory or management experience not required but strongly desired.

Responsibilities

Responsible for, recruiting, consenting, detailing and tracking eligible study subjects for clinical trials
Introduces the details, and parameters of the study to study candidates and appropriate medical staff
Field candidates’ questions and concerns about the study
Obtains signed informed consent from all study participants
Preparation of slides for staining, including cutting paraffin sections (with particular attention to preservation of tissue); sections using patient and control material.
Functions as the liaison between study candidates and the principal investigator
Tracks the number of study candidates that were recruited vs. the number of successful specimen collections
Coordinates pre-operative blood collection handling and storage when required
Collects data, completes Case Report Forms and any required Follow-up Forms
Organizes the maintenance and retention of all study records
Transfers study data confidentially from the study site to Aurora and its clients
Manages inventory for all study supplies
Participates in the collection process and transport preparation of Biospecimens from the Study site to the final destination