Clinical trial monitor Work, Jobs in Oxford (with Salaries)

Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Reading
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
10d
Senior Biomedical Scientist
Deciphex —Oxford
- 8 hour shift
- Management
- Laboratory experience
- Research
- Flexible schedule
Quick apply
Quality Engineer (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Engineering
- Continuous improvement
- Quality control
Quick apply
Principal Investigator
Velocity Clinical Research, Inc. —High Wycombe
- Full-time
- Travel
Quick apply
Medical Monitor (Gastroenterology)
PSI CRO —Oxford
- Full-time
- Remote
- English
- Analysis skills
- Business
Quick apply
Clinical Research Fellow
University of Oxford —Oxford
- £40,190 - £76,582 a year
- Full-time
- University
- Communication skills
9d
Remote Visit Startup Lead
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Business development
- Work from home
9d
Specialist Biomedical Scientist (x2)
Deciphex —Oxford
- 8 hour shift
- Management
- Laboratory experience
- Research
- Annual leave
Quick apply
Clinical Study Manager (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- Leadership
Quick apply
4d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Digital Health Operations Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Presentation skills
- Bachelor's degree
- Leadership
- Work from home
3d
Sr. Manager, Site Budgets and Contracts
Moderna, Inc. —Oxford
- Full-time
- Travel
- Annual leave
Senior Scientist I – Biocompatibility
Abbott Laboratories —Witney
- Full-time
- Microsoft Word
- Doctoral degree
- Engineering
Production Line Lead - PM
Medik8 —Aylesbury
- £30,000 - £33,000 a year
- Monday to Friday
- Computer literacy
- Continuous improvement
- Team management
- Employee discount
Quick apply
3d

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Data Acquisition Specialist - External Data (Remote - UK)

IQVIA -
Reading

Apply Now

Job details

Full-time
10 days ago

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

clinical trial monitor jobs in oxford

Data Acquisition Specialist - External Data (Remote - UK)

Senior Biomedical Scientist

Quality Engineer (Medical Devices)

Principal Investigator

Medical Monitor (Gastroenterology)

Clinical Research Fellow

Remote Visit Startup Lead

Specialist Biomedical Scientist (x2)

Clinical Study Manager (Medical Devices)

Local Study Associate Director

Digital Health Operations Manager - Sponsor Dedicated

Sr. Manager, Site Budgets and Contracts

Senior Scientist I – Biocompatibility

Production Line Lead - PM

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