Назад
Company hidden
2 часа назад

Data Acquisition Specialist - External Data (Remote/Homebased)

Формат работы
remote (только South_africa)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
SA
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Data Acquisition Specialist - External Data (Remote/Homebased) (Clinical Research): Defining, setting up, and ingesting external data streams for clinical trials with an accent on data transfer agreements, data mapping, and regulatory compliance. Focus on implementing transfer mechanisms, validating test data, and resolving data conformance issues with external providers.

Location: Remote/Homebased in Bloemfontein, South Africa

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Define, set up, and ingest standardized and novel external data streams for clinical trials.
  • Assess protocol requirements and plan data stream activities and deliverables for study start-up timelines.
  • Coordinate with data stakeholders and external providers on data transfer, ingestion, structure, and collection requirements.
  • Develop and maintain trial-specific Data Transfer Agreements and create change requests for new test concepts or data structures.
  • Translate medical and scientific concepts into data mapping guidance for clinical programmers.
  • Implement transfer mechanisms, perform UAT of test transfers, and resolve data availability, accuracy, and conformance issues.

Requirements

  • Bachelor’s degree or equivalent, preferably in Computer Science.
  • At least 3 years of experience managing data in support of clinical research.
  • Experience with external clinical data such as safety laboratory, PK, biomarkers, and ECG data.
  • Experience working with external data providers and developing Data Transfer Agreements for clinical studies.
  • Experience working on clinical trials and in diverse, cross-functional, global, and multiregional teams.
  • Knowledge of SDTM, working knowledge of GCP/ICH guidelines, and excellent written and verbal English communication.

Culture & Benefits

  • Remote/home-based work arrangement.
  • Work within global and multiregional clinical research teams.
  • Role supporting the development and commercialization of medical treatments.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →