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13 дней назад

Data Acquisition Specialist (External Data)

Формат работы
remote (только United_kingdom)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
UK
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
Data Acquisition Specialist (External Data) (Clinical Research/Data Management): 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, monitoring data quality, and resolving conformance issues with external providers.

Location: Remote within the United Kingdom; the role is listed in Reading, Berkshire.

Company

hirify.global 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 setup activities to meet study start-up timelines.
  • Create change requests and develop trial-specific Data Transfer Agreements documenting transfer, ingestion, and data structure requirements.
  • Coordinate with clinical data stakeholders and external data providers on data purpose, specifications, transfer frequency, and agreement alignment.
  • Translate medical and scientific concepts into data-mapping guidance for clinical programmers.
  • Perform UAT of test transfers, implement transfer mechanisms into CDR, 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 clinical research.
  • Experience with external clinical data such as safety laboratory, PK, biomarkers, or ECG data, and with external data providers.
  • Experience developing Data Transfer Agreements and working on clinical trials.
  • Knowledge of SDTM and working knowledge of GCP/ICH guidelines.
  • Excellent written and verbal English communication; UK visa sponsorship is not available.

Culture & Benefits

  • Work remotely from within the United Kingdom.
  • Collaborate with diverse, cross-functional, global, and multiregional clinical research teams.
  • Contribute to the development and commercialization of medical treatments and improved patient outcomes.

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