Ssa Data Measurement & Martech Lead (Salesforce) - Hybrid

Jobs2Web; Gauteng; Remote; ZAR 420,000 - 620,000; Full time

Job summary

Jobs2Web is seeking a Data Acquisition Specialist for External Data (Remote/Homebased) to define and ingest external data streams for clinical trials. You will work with labs, ECG, biomarker, EHR and wearables sources, ensuring compliant data transfer and mapping per protocol.

The role requires 3+ years in clinical data management, familiarity with SDTM, GCP/ICH, and strong English communication, across diverse cross-functional teams. Remote work supports multi-region collaboration.

Qualifications

• Bachelor's degree or equivalent, preferably in Computer Science.
• Minimum of 3 years' experience managing data in clinical research.
• Experience with external data sources in clinical studies.
• Experience developing data transfer agreements.
• Experience in clinical trials and cross-functional, global teams.
• Knowledge of SDTM and GCP/ICH guidelines.
• Excellent written and verbal English communication.

Responsibilities

• Define, set up and ingest External Data Streams per protocol.
• Coordinate with data stakeholders on transfer, ingestion and structure of data.
• Create change requests for new data concepts.
• Develop trial-specific data transfer agreements (tsDTAs).
• Ensure data transfer frequencies meet study timelines.
• UAT of test data transfers and data specifications alignment.
• Monitor external data stream availability and data accuracy.

Skills

Data management

Communication

English proficiency

Education

Bachelor's degree or equivalent

Tools

SDTM

GCP/ICH guidelines

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 with external data providers within a clinical study setting.
• Experience developing data transfer agreements.
• Experience working on clinical trials.
• Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional.
• Knowledge of SDTM.
• Working knowledge of GCP/ICH guidelines
• Excellent written and verbal communication in English.

EEO Statement

EEO Minorities/Females/Protected Veterans/Disabled