Data programmer Work, Jobs in Bagshot, Sry (with Salaries)

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Health Economic Expert (UK Posting)
UCB —Slough
- Doctoral degree
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The Royal Marsden NHS Foundation Trust —Chelsea
- £47,951 - £56,863 a year
- Full-time
- Communication skills
4d

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Data Acquisition Specialist - External Data (Remote - UK)

IQVIA -
Reading

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Computer Science
Stakeholder collaboration
Stakeholder liaison
English
Bachelor's degree
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Communication skills
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Reading, United Kingdom | Full time | Home-based | R1560752

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.

This role is not eligible for UK visa sponsorship

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 https://jobs.iqvia.com

IQVIA 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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

data programmer jobs in bagshot, sry

Data Acquisition Specialist - External Data (Remote - UK)

Programmer Analyst

Data - Programmer

Statistical Programmer

Database Manager and Scientific Programmer

Sr. Clinical Data Manager (Netherlands, United Kingdom)

Clinical Data Manager - FSP (Homebased - UK)

Senior Clinical Data Manager - sponsor dedicated - oncology

Senior Technical Designer - Medidata RAVE Certification required

Senior Statistical Programmer - Sponsor Dedicated

Senior Principal Programmer (UK)

Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated

Pharmacometrics Support Programmer

DM/STDM Programmer

Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

Lead Statistical Programmer - Sponsor Dedicated

Principal Statistical Programmer - Sponsor Dedicated, EMEA

Freelance Clinical Database Programming Process Lead

Health Economic Expert (UK Posting)

Trial Manager

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