Data Acquisition Specialist - External Data (Remote/Homebased)
Контакты
Формат работы
remote (только South_africa)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
SA
gcpclinical researchdata mappingclinical trialsich guidelinessdtmexternal datadata transfer agreements
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата не указанаСтабильный доменЧеткий фокусПроф. стандарты
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Data Acquisition Specialist - External Data (Remote/Homebased) (Clinical Research/Data Management): Defining, setting up, and ingesting external data streams for clinical trials, including laboratory, imaging, biomarker, genomic, EHR, wearable, and sensor data, with an accent on data transfer agreements, data mapping, and regulatory compliance. Focus on coordinating providers and stakeholders, implementing transfer mechanisms, validating test transfers, and resolving data conformance issues.
Location: Remote/Homebased, Bloemfontein, South Africa
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 study-specific external data streams aligned with clinical trial protocol requirements.
Assess external data collection requirements and plan stream setup activities and deliverables for study startup timelines.
Coordinate with data stakeholders and external providers on data transfer, ingestion, structure, frequencies, and applicable data protection requirements.
Create change requests for new test concepts and data structures, and develop accurate trial-specific Data Transfer Agreements.
Translate medical and scientific concepts into data mapping guidance and perform UAT of test data transfers.
Implement transfer mechanisms into CDR, monitor data availability and accuracy, and resolve conformance issues with providers.
Requirements
Bachelor’s degree or equivalent, preferably in Computer Science.
At least 3 years of experience managing data in support of clinical research.
Experience working with external data such as Safety Lab, PK, simple biomarkers, or ECG data.
Experience working with external data providers within a clinical study and developing data transfer agreements.
Experience working on clinical trials and in highly diverse, cross-functional, global, and multiregional clinical research teams.
Knowledge of SDTM and working knowledge of GCP/ICH guidelines.
Excellent written and verbal communication in English.
Culture & Benefits
Remote/homebased work arrangement.
Work within global and multiregional clinical research teams.
Focus on integrity and truthful, complete candidate information throughout the hiring process.
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