Private Client Wealth Advisor - Education & Growth

Rmb Nigeria Limited; South Africa; Remote; ZAR 480,000 - 720,000; Full time

Job summary

Rmb Nigeria Limited is seeking a Data Acquisition Specialist - External Data (Remote/Homebased) to define, set up and ingest external data streams for clinical trials. You will work with central labs, ECG, real world data sources and other digital data sources to ensure compliant data capture and transfer.

The role requires 3+ years in data management for clinical research, and a Bachelor's degree in Computer Science.

Qualifications

• Bachelor's degree or equivalent in a relevant field (prefer CS).
• 3+ years' experience managing data in clinical research.
• Experience with external data sources (ECG, labs, biomarkers).

Responsibilities

• Execute deliverables for Standardized External Data Streams.
• Plan external data set-up to meet study start-up timelines.
• Liaise with data stakeholders to define data transfer requirements and structure.
• Create tsDTA documents for data transfer and ingestion.
• Ensure data transfer frequencies meet study requirements.
• UAT of data transfers to ensure accuracy and consistency.
• Monitor external data streams availability and resolve data issues.

Skills

Data management

Stakeholder liaison

Data mapping

UAT testing

Education

Bachelor's degree in Computer Science

Tools

CDR (Clinical Data Repository)

Job description

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
• Experience in working