CLINICAL RESEARCH TECH ADVANCED

SPAULDING CLINICAL RESEARCH LLC•West Bend, WI

5d•$20 - $25•Onsite

About The Position

SPAUDING CLINICAL aims to be the clinical research organization by which all others are measured. Pioneering in our approach to redefining how the industry perceives and achieves success; passionate in our pursuit of ingenious solutions that mitigate risk; loving in our care for our volunteers, customers and employees; and heroic in our ambitions to ensure the health and safety of people around the globe - Spaulding Clinical is taking research beyond results to create a marketplace of safer drugs. SPAULDING CLINICAL is looking for a Clinical Research Technician - Advanced to join our AM Team! Position Snapshot Full-time Onsite Monday – Friday, Hours are between (7am – 3:30pm) Ability to work every other holiday rotation and weekend rotation Health, Dental, Vision, Life, Long/Short Term Disability, and Supplemental insurance options 401k Paid Time Off / Holiday Pay Required Training: Training will begin starting your first two days of New Hire Orientation, which will be a Monday and a Tuesday from 8a-4:30p. Training would continue on Wednesday through Friday 8AM - 4:30PM for your first week. Starting week #2, the training start time may vary between the hours of 6AM and 8AM Monday-Friday, to get signed off on events but are still 8-hour shifts on AM Shift. Training takes a minimum of 8 weeks on this AM schedule before you would switch to your offered shift.

Requirements

Ability to read, write and interpret the English language.
Portrays professionalism in all interactions at Spaulding Clinical.
Good computer skills; inclination to adopt technology to maximize efficiency
Demonstrates strong analytical, problem solving skills
Strong written and verbal communication skills.
Detail oriented, good organizational traits.
Self-motivated
Must be results-oriented, multi-tasking, quick learner, respond to the urgent needs of the team, and show a strong track record of meeting deadlines.
Ability to work beyond normal work hours and various shift availability required.
Ability to perform and record data entry via computer systems while conducting timed clinical procedures.
Phlebotomy Certificate or associated real-world (on-the-job training) experience required
BLS certification required within 6 months of hire or promotion date

Nice To Haves

Associate's Degree in a scientific/medical discipline desirable
Certified Nursing Assistant or Medical Assistant certification highly desirable

Responsibilities

Responsible for advanced technical procedures (such as, but not limited to, meal administration, subject positioning, bag check, vital signs, ECG lead placement, phlebotomy, urine collection, PK runner, height/weight/BMI, dose verification) in the conduct of clinical trials with emphasis on the safety and welfare of study participants.
Performs the practical activities of clinical studies according to protocol, regulatory requirements, SOPs, scope of practice and current training status.
Ensures that clinical trials are conducted according to protocol requirements by utilizing the following techniques & procedures.
Performs meal administration, ensuring the correct meal and correct content is delivered to the correct study participant.
Performs subject bag checks to ensure no contraband is present on study floor
Performs study activities such as ECG positioning, exercises, or other study procedures requiring supervision of subjects.
Performs venipuncture, capillary, and/or IV specimens from study subjects according to established protocol, maintains aseptic technique.
Performs proper and accurate sample management, including collection, identification, transport, and/or processing of biological (blood, urine, etc) subject samples.
Performs dose verification, assisting Clinical Research Nurses during dose administration to accurately verify subject identity and dosing labeling, as additional quality check.
Report any subject complaints of adverse events immediately to Charge staff or Clinical Research Nurses to ensure appropriate evaluation and treatment.
Performs and records physical measurements including height, weight, and BMI calculation.
Performs and records vital sign measurements (blood pressure, pulse oximetry, heartrate, temperature, respirations, etc).
Places ECG electrodes and leads accurately to ensure precise telemetry monitoring.
Performs additional task list items as delegated and supervised by Charge Staff.
Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study procedures, as they apply to their role and ensures that Delegation of Authority/Training Log for each study is completed in a proper and timely manner.
Keeps abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines, state and national laws and ethical standards.
Observes and maintains all HIPAA, OSHA, and Exposure Control regulations and Emergency Response as required by applicable training.
Creates and maintains accurate records of all protocol activities and events, as delegated and trained.
Follows progress of volunteers and provides for their care, comfort and safety by attending to their needs during study participation.
Participates in quality assurance of clinical research projects and initiates the need for same as it impacts on clinical practice.