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3 часа назад

Clinical Research Assistant II

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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Описание вакансии

Текст:
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TL;DR
Clinical Research Assistant II (Clinical Research): Supporting coordinators with clinic procedures, study preparation, documentation, and participant interactions with an accent on GCP compliance, protocol adherence, and administrative accuracy. Focus on assisting with informed consent, assessments, instrumentation and photography, quality-checking study documents, and coordinating multiple tasks in a fast-paced clinic environment.

Location: Richardson, Texas, USA; onsite

Company

SGS is a global testing, inspection and certification company focused on sustainability, quality and integrity.

What you will do

  • Assist study coordinators with daily clinic procedures, including electronic self-assessment questionnaires, check-ins, informed consent, instrumentation and photography.
  • Support study preparation and conduct through test material preparation, appointment reminders and quality checks of study documents.
  • Assist with developing study paperwork and perform tasks for other departments as needed.
  • Follow Good Clinical Practice guidelines, applicable regulations, standard operating procedures and work instructions.
  • Provide respectful customer service to clients and panelists while maintaining positive interactions with colleagues and leadership.
  • Follow safety and Operational Integrity procedures and processes.

Requirements

  • Associate degree or at least one year of administrative or clerical work experience.
  • Strong attention to detail, organizational skills, verbal and written communication skills, and interpersonal skills.
  • Ability to follow study protocols and instructions according to GCP guidelines, applicable regulations and SOPs.
  • Ability to report to the clinic on time for assigned studies.
  • Ability to lift moderately heavy items and coordinate multiple projects in a fast-paced professional environment.

Nice to have

  • CCRC or CCRA certification.

Culture & Benefits

  • Full-time employment.
  • Work within a global network of testing, inspection and certification offices and laboratories.
  • Equal opportunity employment and reasonable accommodation support.

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