Bar Steward - Cruise Beverage Specialist

Princess Cruise Line; Cape Town; À distance; ZAR 360 000 - 480 000; Plein temps

Résumé du poste

Princess Cruise Line is hiring a Data Acquisition Specialist - External Data (Remote/Homebased) to manage the setup and ingestion of diverse external data streams for clinical trials. You will coordinate with labs, imaging, EHR, wearables, and other digital sources, ensuring compliant data transfer and proper mapping.

You will draft Data Transfer Agreements, perform UAT, and monitor data availability and quality across streams, while liaising with stakeholders to meet protocol timelines.

Qualifications

• Bachelor's degree or equivalent, preferably in Computer Science.
• Minimum of 3 years' experience managing data in support of clinical research.
• Experience with external data e.g., ECG, labs, imaging, EHR, wearables is advantageous.

Responsabilités

• Execute deliverables for Standardized External Data Streams.
• Assess external data collection requirements per protocol and plan setup activities to meet study timelines.
• Liaise with data stakeholders to define data transfer, ingestion, and structure per data models.
• Create change requests for defining new data concepts or structures.
• Develop trial-specific Data Transfer Agreements documenting study requirements and methods.
• Ensure data transfer frequencies meet study requirements (monitoring and reporting).
• Liaise with external data providers to align on tsDTA.
• Translate medical concepts into data mapping guidance for clinical programmers.
• UAT of test data transfers to ensure alignment with data specifications.
• Implement data transfer mechanisms into the data repository (CDR).
• Monitor availability and accuracy of external data streams with providers.

Connaissances

Data mapping

Data transfer

Stakeholder liaison

UAT testing

External data streams

Documentation

Change requests

TDTA development

Formation

Bachelor's degree in Computer Science

3+ years data management in clinical research

Description du poste

Data Acquisition Specialist - External Data (Remote/Homebased)

Bloemfontein, South Africa
Durban-Inland, KZN, South Africa
Centurion, South Africa
Bellville, South Africa
Full time
R
The Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture.
External data streams include but are not limited to typical and novel data collected through central labs and ECG, medical imaging, biomarker and genomics analysis, real world data sources, EHR, electronic patient reported outcomes, wearables and sensors and other digital data collection technologies.
Deliverables

• Execute deliverables for Standardized External Data Streams.
• Assess external data collection requirements per protocol and planning of external data stream set-up activities and related deliverables to meet study start‑up timelines.
• Liaise with key data stakeholders to establish the purpose of data collection and requirements for the transfer, ingestion, and structure of data for each data stream in compliance with applicable data protection laws and regulations, utilizing available standards and templates
• Create change requests for the definition of new test concepts or data structures relating to external data.
• Develop trial‑specific Data Transfer Agreements (tsDTA's) accurately documenting study requirements and methods for the data transfer, ingestion, and structure.
• Ensure data transfer frequencies are sufficient for the agreed requirements (medical data review, central monitoring, and reporting and analysis).
• Liaise with external data providers to ensure alignment and agreement of tsDTA.
• Translate medical and scientific concepts into data mapping guidance, per agreed data model and documented in the annotated Data Transfer Agreement for use by Clinical programmers.
• UAT of test data transfers ensure accuracy and consistency with data specifications defined in Data Transfer Agreements.
• Implement data transfer mechanisms for external data streams (into CDR) including access for external data providers.
• Monitor availability and accuracy of external data streams, liaise with external data providers to resolve data transfer issues relating to conformance of data.

Education and Experience Requirements

• Bachelor's degree or equivalent, preferably in Computer Science.
• Minimum of 3 years' experience managing data in support of clinical research.
• Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG, etc