Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
AT
Alchemy Trials
Medical Assistant
Entry-Level JobVerifiedNo experience needed
Career Insights for Medical Assistant
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Florida data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Medical Assistant assists physicians and other medical specialists with routine administrative or clinical tasks. Organizes patient records, schedules appointments, and prepares medical equipment. May specialize in administrative or clinical work, or specialize in a particular area of medicine, i.e. assisting in the office of an ophthalmologist (eye specialist). Works in medical offices.
$36,747 / year median in Florida
+21% projected growth
Job Description
Medical Assistant Alchemy Trials Hialeah, FL Job Details Full-time From $18 an hour 9 hours ago Qualifications Good Clinical Practice (GCP) High school diploma or GED Certified Medical Assistant Full Job Description Clinical Research Assistant Alchemy Trials is a Florida-based Site Management Organization (SMO) supporting clinical trials across high-volume community medical practices, with a focus on medical device, IVD, point-of-care (POC), OTC, and diagnostic studies. Our embedded research model combines on-site research personnel with centralized regulatory, operational, and quality oversight. Position Summary We are seeking a motivated and detail-oriented Clinical Research Assistant to support Clinical Research Coordinators and Principal Investigators in the day-to-day execution of clinical research studies. This is an excellent opportunity for an individual looking to develop hands-on experience in clinical research. Key Responsibilities Assist Clinical Research Coordinators with daily study activities Support participant recruitment, pre-screening, and scheduling Maintain study documents, subject files, and regulatory documentation Assist with data entry and source documentation Support informed consent and study visit workflows under appropriate supervision Prepare study materials and supplies for participant visits Assist with collection, processing, labeling, storage, and shipment of clinical specimens as trained and delegated Maintain study equipment and temperature logs Assist with sponsor/CRO monitoring visits and site preparation Follow study protocols, site SOPs, ICH-GCP, HIPAA, and applicable regulatory requirements Promptly escalate protocol, documentation, or participant-related concerns to the Clinical Research Coordinator Qualifications High school diploma required; associate or bachelor's degree in a healthcare or science-related field preferred Medical Assistant, phlebotomy, or healthcare experience is a plus Clinical research experience is preferred but not required Strong organizational skills and attention to detail Comfortable working with patients and clinical staff Strong written and verbal communication skills Ability to manage multiple tasks in a fast-paced clinical environment Basic computer and electronic documentation skills What We're Looking For The ideal candidate is dependable, organized, professional, and eager to build a career in clinical research. We value individuals who take initiative, follow procedures carefully, and understand the importance of participant safety, protocol compliance, and data integrity. To Apply Please submit your resume through Indeed. Candidates with medical assisting, phlebotomy, laboratory, patient-care, or clinical research experience are encouraged to apply.