Research Medical Assistant

Encino, California

Employer: Medix
Industry: Life Sciences
Salary: Competitive
Job type: Part-Time
Are you a Medical Assistant ready for your next career opportunity? Look no further, this is the PERFECT opportunity for a healthcare professional to break into the clinical research industry and impact the lives of communities across the globe.

Experience as a Medical Assistant is a MUST HAVE.

Important Information:
  • Location: Must reside locally in Encino, CA 91316
  • Contract Duration: September 3, 2024 - December 20, 2024; contract duration is subject to change
  • Schedule: PART TIME, 2-3 days per week (16-24 hours per week); days worked is up to the candidate.
  • Clinic is open Monday-Friday 8:00am-5:00pm


Role & Responsibilities:
  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and site's SOPs
  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • Enter source data into the sponsor's and/or vendor's data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
  • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
  • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
  • Maintain confidentiality of patient protected health information, sponsor confidential information and site confidential information
  • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • Prepare source document charts, copy and/or file medical records and study related documents as required.
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • Other duties as assigned
Created: 2024-08-27
Reference: 232312_1724686231
Country: United States
State: California
City: Encino

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