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10 дней назад

Clinical Research Assistant - MA, EMT, CPT, or LVN/LPN Preferred (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Clinical Research Assistant (Clinical Research): Supporting clinical trial execution at an on-site research facility with an accent on participant safety, protocol compliance, sample handling, and accurate clinical data collection. Focus on assisting with phlebotomy, clinical assessments, EDC documentation, study visit preparation, and regulatory filing under GCP and site procedures.

Location: On-site in Chattanooga, Tennessee, USA

Company

hirify.global Wake Research is a multi-site clinical research organization conducting clinical trials for biopharmaceutical, biotechnology, medical device, pharmaceutical, and CRO partners.

What you will do

  • Maintain clinical supplies, exam rooms, laboratory spaces, equipment logs, and temperature records.
  • Assist with phlebotomy, sample processing, and preparation and shipment of biological specimens according to protocols and IATA requirements.
  • Prepare participant charts, lab kits, requisitions, and study documentation for clinical visits.
  • Perform delegated clinical procedures such as vital signs, ECGs, and PFTs.
  • Collect, document, and enter participant data in source records and EDC systems; assist with queries and eDiary reconciliation.
  • Support participant scheduling, follow-up communications, regulatory filing, and protocol compliance in collaboration with clinical research staff.

Requirements

  • At least two years of experience in a healthcare setting.
  • Previous experience as a medical assistant, EMT, LPN, or LVN; phlebotomy experience is highly preferred.
  • Ability to understand complex protocols, follow detailed instructions, learn quickly, and manage multiple tasks.
  • Strong verbal and written communication skills and interpersonal skills.
  • Ability to maintain patient, employee, and company confidentiality and follow HIPAA guidelines.
  • Prior clinical research experience is preferred.

Culture & Benefits

  • Full-time employment in an on-site clinical research environment.
  • Training includes GCP, OSHA, IATA, and site standard operating procedures.
  • Health, dental, vision, life, and disability insurance.
  • 401(k) with matching, paid time off, flexible spending account, and employee assistance program.

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