Checkout Pro - Fast, Friendly Packing Specialist

Papenfus Retail Consultants Cc

Upington

Teletrabalho

ZAR 550 000 - 750 000

Tempo integral

Há 7 dias
Torna-te num dos primeiros candidatos

Recebe uma resposta deste empregador

O teu currículo e carta de apresentação, adaptados exatamente ao que estão a contratar.

Ultrapassa os filtros ATS

Resumo da oferta

IQVIA seeks a Data Acquisition Specialist to manage external data streams in clinical studies. You will define data capture processes, liaise with data stakeholders and ensure compliant transfer, ingestion, and structure of diverse data sources including labs, ECG, imaging, and digital data.

You will draft tsDTA documents, oversee data transfer frequencies for central monitoring, and support clinical programmers with data mapping.

Qualificações

  • Bachelor's degree or equivalent, preferably in Computer Science.
  • Minimum of 3 years' experience managing data in support of clinical research.
  • Knowledge of SDTM and GCP/ICH guidelines.
  • Excellent written and verbal communication in English.

Responsabilidades

  • Define, set-up and ingest External Data Streams per protocol requirements.
  • Liaise with data stakeholders for data transfer, ingestion and structure.
  • Develop Data Transfer Agreements (tsDTA) documenting study requirements.
  • Ensure data transfer frequencies meet monitoring and reporting needs.
  • Translate medical concepts into data mapping guidance for Clinical programmers.
  • UAT of test data transfers for accuracy against data specifications.

Conhecimentos

Data management
Clinical data
Communication

Formação académica

Bachelor's degree in Computer Science
3+ years clinical data experience

Descrição da oferta de emprego

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

Obtém a tua avaliação gratuita e confidencial do currículo.

ou arrasta e larga o ficheiro aqui.

Similar jobs

Ofertas semelhantes que vale a pena comparar

Fa Specialist Stores
Fa Specialist Stores

Samancor Chrome Ltd. • África do Sul

Teletrabalho
ZAR 550 000 - 900 000
Tender Specialist
Tender Specialist

Ideal And Selected Candidates • África do Sul

Teletrabalho
ZAR 420 000 - 780 000
Ice Cream Cart Specialist — Evenings & Weekends
Ice Cream Cart Specialist — Evenings & Weekends

Wild Dreams Hospitality • Stellenbosch

Teletrabalho
ZAR 480 000 - 760 000
Omf Client Relations Consultant (Mthatha Plaza)
Omf Client Relations Consultant (Mthatha Plaza)

Old Mutual South Africa • Oos-Kaap

Teletrabalho
ZAR 550 000 - 850 000
Senior Sap Successfactors Ec & Time Management Consultant
Senior Sap Successfactors Ec & Time Management Consultant

Dearx • Stellenbosch

Teletrabalho
ZAR 480 000 - 720 000
Africa-Focused Financial Advisor | Consultative Selling
Africa-Focused Financial Advisor | Consultative Selling

Old Mutual Life Assurance Company • África do Sul

Teletrabalho
ZAR 550 000 - 850 000
Farm Machinery Technician: Field & Workshop Specialist
Farm Machinery Technician: Field & Workshop Specialist

Placements24 • KwaZulu-Natal

Teletrabalho
ZAR 600 000 - 800 000
Elite Automotive Detailing Specialist
Elite Automotive Detailing Specialist

Placements24 • Mbombela (Nelspruit)

Teletrabalho
ZAR 400 000 - 700 000
Mine Environmental Officer
Mine Environmental Officer

Placements24 • África do Sul

Teletrabalho
ZAR 420 000 - 660 000
Property Debt Recovery Specialist
Property Debt Recovery Specialist

Trafalgar • East London

Teletrabalho
ZAR 500 000 - 900 000