CLINICAL RESEARCH TECHNICIAN

SPAULDING CLINICAL RESEARCH LLC•West Bend, WI

10d•Onsite

About The Position

NOW HIRING: Clinical Research Technician Phlebotomy & Clinical Trials Starting Pay: $23.00 per hour, also offering a $5,000 sign-on bonus after 90 days of continuous employment in good standing. Fast-Paced Clinical Research Environment Career Growth & Advancement Opportunities in Healthcare & Research Are you a skilled phlebotomist or healthcare professional who enjoys a fast-paced environment, continuous learning, and meaningful work? Join our clinical research team and gain valuable experience supporting clinical trials alongside healthcare and research professionals. This role is ideal for: Phlebotomists EMTs Nursing or Pre-Med Students Healthcare professionals looking to expand into clinical research.

Requirements

Experienced or certified in phlebotomy
Comfortable working in fast-moving clinical settings
Detail-oriented and dependable
Strong communicators and team players
Interested in expanding their healthcare and research experience
Able to multitask and adapt throughout the day
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

Collect blood samples through venipuncture and specimen collection
Record vital signs, height, weight, and BMI
Place ECG leads and electrodes
Assist with participant safety and monitoring
Support medication dose verification procedures
Collect urine samples and perform drug screenings
Ensure study procedures are completed according to protocol and safety guidelines
Maintain accurate clinical documentation and records
Help provide a safe, comfortable, and professional experience for study participants
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.
As required for study or site needs and if trained and delegated may be assigned study procedures such as obtaining participant information/histories/questionaries/meals/vital signs/EKGs/drug administration/specimen collection/luggage searches.