CLINICAL MEDICAL ASSISTANT

SPAULDING CLINICAL RESEARCH LLC•West Bend, WI

4d•Onsite

About The Position

START YOUR HEALTHCARE CAREER — NO EXPERIENCE NEEDED NOW HIRING: Clinical Medical Assistants Entry-Level Healthcare Position Starting Pay: $16.00/hour -Perfect for High School Seniors, College Students & Future Healthcare Professionals -Paid Training Provided -No Certification Required -No Experience Needed Looking for a way to start a career in healthcare? Join our clinical research team and gain hands-on experience working alongside nurses, medical assistants, and research professionals in a fast-paced clinical environment. This opportunity is great for: High school graduates and seniors College or nursing students Individuals exploring a healthcare career Career changers Anyone looking to gain medical experience Whether you’re planning a long-term healthcare career or simply looking for meaningful work with growth opportunities, we provide the training to help you succeed.

Requirements

Positive attitude and willingness to learn
Strong communication and teamwork skills
Interest in healthcare or clinical research
Reliable and professional work ethic
Ability to read, write and interpret the English language.
Portrays professionalism in all interactions at Spaulding Clinical.
Proficient 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.
Ability to sit, stand, walk, reach with hands and arms, and use hands along with fingers, to handle or feel.
Ability to lift and/or move up to 25 pounds.
Specific vision abilities required by this job include clarity of vision both near and far.
Ability to identify and distinguish colors.

Nice To Haves

BLS certification preferred within 6 months of hire or promotion date.

Responsibilities

Take vital signs and perform basic technical procedures
Position study participants and assist with meal administration
Perform urine collection and drug screening
Place ECG (electrocardiogram) electrodes and leads
Conduct bag checks and support participant safety
Follow study protocols, Standard Operating Procedures (SOPs), and safety guidelines
Help ensure the comfort, safety, and wellbeing of study participants
Assist with patient care activities during clinical trials
Performs meal administration, ensuring the correct meal and correct content is delivered to the correct study participant.
Performs participant bag checks to ensure no contraband is present on study floor.
Performs study activities such as vital signs and ECG positioning, or other study procedures requiring supervision of study participants.
Performs and records vital sign measurements (blood pressure, pulse oximetry, heart rate, temperature, respirations, etc.).
Performs urine collection for drug screen and analysis, ensuring proper instructions for sample are given to participants and proper sample requirements are met.
Places ECG electrodes and leads accurately and performs quality check 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 participants 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.