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Assistant Iata Jobs (NOW HIRING)

DM Clinical

Research Assistant I (3656)

Irving, TX · On-site

$18.50 - $25.50/hr

Completing DMCR-required training, including GCP and IATA. * Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study ...

DM Clinical

Research Assistant III (3659)

Sugar Land, TX · On-site

$17.25 - $24/hr

Completing DMCR-required training, including GCP and IATA. * Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study ...

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Assistant Iata information

What is the difference between Assistant Iata vs Travel Agent?

AspectAssistant IataTravel Agent
CredentialsTypically requires IATA certification, basic travel industry knowledgeOften requires IATA certification, travel diploma, or relevant experience
Work EnvironmentAirlines, travel agencies, or corporate travel departmentsTravel agencies, online platforms, or independent
Industry UsageUsed mainly within airline and airline-related sectorsUsed broadly across travel and tourism industry

The Assistant Iata and Travel Agent roles both require IATA certification and involve working within the travel industry. However, Assistant Iata positions are often more focused on airline operations and support, while Travel Agents handle customer bookings, travel planning, and client service. Both roles serve the travel industry but differ in daily responsibilities and work environments.

What cities are hiring for Assistant Iata jobs? Cities with the most Assistant Iata job openings:
What are the most commonly searched types of Iata jobs? The most popular types of Iata jobs are:
What states have the most Assistant Iata jobs? States with the most job openings for Assistant Iata jobs include:
Assistant Iata jobs near you
Clinical Research Assistant

Clinical Research Assistant

DERMCARE MANAGEMENT LLC

Dallas, TX • On-site

Full-time

Posted 22 days ago

Job description

Clinical Research Assistant will perform work in one or all of the following areas Phlebotomy, Data Entry, and Administrative Assistant responsibilities in support of the clinical research team. The Clinical Research Assistant will assist in the management of multiple clinical trials according to the study protocol, perform collection of clinical data points, and provide seamless customer service to the patients attending the site.

Responsibilities Include but not limited to:

  • Complete training and ensure adherence of GCPs, SOPs, IATA, and HIPPA
  • Ensure compliance with all clinical trial protocols
  • Ensure compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC, and HIPPA.
  • Assist research staff with Phase II-IV clinical trials from start through closure
  • Enter visits, patient recruitment in Real Time Clinical Trial Management System (CTMS)
  • Aid research department is meeting contracted and expected recruitment goals
  • Engage in quality assurance of all study documents and data prior to monitoring visits
  • Support central and local marketing campaigns by entering recruitment data, contacting patients and scheduling.
  • Coordinate office visits for trial participants based on the protocol
  • Perform phlebotomy, collect, process and ship clinical specimens
  • Assist in patient care visits and procedures according to protocol
  • Receive medication, confirm temperature in range and maintain temperature logs
  • Perform ECGs
  • Engage in patient recruitment
  • Assist with entry into Electronic Data Capture (EDC) data queries are resolved
  • Participate in Investigator meetings and trainings during the course of the trial
  • Generate PowerPoint presentations
  • Create and organize new patient charts, lab and other required supplies prior to the patient visit.
  • Gain access to Institutional Review Boards.
  • Maintain regulatory binders, CRFs, subject charting, and source documents
  • Maintain the Investigator Site Files
  • Assist with keeping Institutional Review Boards (IRB) documents, Electronic Data Capture (EDC) Clinical Trials Management System (CTMS) and Interactive Web Response Systems (IWRS) current
  • Will support central and local marketing campaigns by contacting potential subjects and scheduling
  • Possess a minimum of two (2) years experience in the clinical research or closely related field
  • Bachelors degree or relevant work experience.
  • Bilingual (Spanish), a plus.

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