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  3. Phlebotomist (3781)
Job detail

Phlebotomist (3781)

DM CLINICAL RESEARCH GROUP

Employer page
#Medical Terminology#Certified Medical Assistant#Specimen Collection#Phlebotomist#Clinical Research#Informed Consent#Patient Data#Adverse Events#EDC System
#Investigator Brochures
OtherOn Site0-2 yrsPosted 3 days agoCloses Jul 27

Location

Irving, Texas

Quick overview

The Phlebotomist assists clinical research staff by collecting and recording patient data and managing the shipment of specimens. They are also responsible for conducting patient visits and reporting adverse events according to sponsor requirements.

Requirements summary

A high school diploma is required, while phlebotomy or medical assistant certifications are preferred. Candidates must have knowledge of medical terminology and strong attention to detail.

high schoolprofessional certificateCustomer ServicePhlebotomyMedical TerminologyComputer SkillsClinical ResearchPatient Data CollectionSpecimen ManagementEDC SystemsAudit ResolutionPatient Visit Coordination

Job description

Job DetailsJob Location

  • Dallas, TX - Irving, TX 75061The Phlebotomist (or Certified Medical Assistant) will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIES Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system. Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start. Maintaining clear, concise, accurate, and legible records. Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s). Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s). Conducting patient visits. Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor. Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner.
  • Knowledge &
  • Experience
  • Education:
  • High school diploma or equivalent required
  • Experience: Prior experience in clinical research is not required but preferred
  • Credentials: Phlebotomist certificate preferred
  • Medical
  • Assistant
  • Certification preferred
  • Knowledge &
  • Skills: Knowledge of medical terminology required Must be detail-oriented and demonstrate attention to detail Excellent customer service skills Excellent computer skills Qualifications

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DM CLINICAL RESEARCH GROUP

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Hiring organization

DM CLINICAL RESEARCH GROUP

DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified...

Explore employer profile
IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
HQHouston, TX
Founded2006
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