Ally Bradley
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Ally Bradley Email & Phone Number

Project Manager - Software Solutions at IQVIA
Location: Oxford, England, United Kingdom 13 work roles 3 schools
1 work email found @nds.ox.ac.uk LinkedIn matched
✓ Verified Jul 2026 4 data sources Profile completeness 100%

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Current company
Role
Project Manager - Software Solutions
Location
Oxford, England, United Kingdom
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Who is Ally Bradley? Overview

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Quick answer

Ally Bradley is listed as Project Manager - Software Solutions at IQVIA, a with 52333 employees, based in Oxford, England, United Kingdom. AeroLeads shows a work email signal at nds.ox.ac.uk and a matched LinkedIn profile for Ally Bradley.

Ally Bradley previously worked as electronic Clinical Outcome Assessments at Iqvia and Senior Global Trial Manager at Iqvia. Ally Bradley holds Materials Engineering from University Of Wales, Swansea.

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*@nds.ox.ac.uk
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Profile bio

About Ally Bradley

Ally Bradley is a Project Manager - Software Solutions at IQVIA. She possess expertise in clinical trials, data management, gcp, clinical research, clinical research governance and 29 more skills.

Listed skills include Clinical Trials, Data Management, Gcp, Clinical Research, and 30 others.

Current workplace

Ally Bradley's current company

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IQVIA
Iqvia
Project Manager - Software Solutions
Oxford, GB
Website
Employees
52333
AeroLeads page
13 roles

Ally Bradley work experience

A career timeline built from the work history available for this profile.

Project Manager - Software Solutions

Oxford, Gb

Project Manager - Software Solutions

Current

United Kingdom

Oct 2024 - Present

Electronic Clinical Outcome Assessments

Oxford, England, United Kingdom

Jan 2022 - Oct 2024

Senior Global Trial Manager

Sep 2020 - Jan 2022

Clinical Trials Unit Coordinator

Oxford, United Kingdom

Jan 2018 - May 2019

Cope Trials Central Manager

Oxford, United Kingdom

COPE (Consortium for Organ Preservation in Europe) is an EU funded programme of research work incorporating clinical trials, translational experiments, creation of a BioBank for clinical samples and an information dissemination programme. I work with clinical teams and businesses across Europe including Belgium, The Netherlands, France, Germany and Spain.Responsibilities:• Set-up and oversight of all management for the clinical trials and biobank • Negotiation with legal… Show more COPE (Consortium for Organ Preservation in Europe) is an EU funded programme of research work incorporating clinical trials, translational experiments, creation of a BioBank for clinical samples and an information dissemination programme. I work with clinical teams and businesses across Europe including Belgium, The Netherlands, France, Germany and Spain.Responsibilities:• Set-up and oversight of all management for the clinical trials and biobank • Negotiation with legal representatives to satisfy complex contractual issues between business partners, study sponsor and research sites• Oversee REC and R&D submissions• Develop site monitoring systems and documentation• Develop and deliver site initiation and training programme • Create and implement site monitoring plans • Monitor SAEreporting and ensure they are followed up appropriately• Develop good communication avenues with sites and project partner companies• Ensure adherence to study protocols, research governance, regulatory requirements and GCP• Member of the COPE Management Board and chair of project management and study specific internal and external meetings• Advise management board and research teams on strategic planning and logistical processes• Assess training needs at sites and arrange additional training as required• Produce and present progress reports to senior boards/committees• Ensure research teams and site staff comply with ICH-GCP and CT Regulations• Support and advise staff on research specific requirements (research passports, DBD checks, occupational health)• Monitor and manage data and sample collection and resolve discrepancies• Design and develop data collection and reporting facilities tools• Encourage site staff to provide accurate and timely data entry • Establish and monitor systems to assess data quality and completeness• Represent COPE and contribute to industrial partner strategy meetings Show less

Mar 2013 - Apr 2015

Expert Trial Manager

Primary Health Care Sciences

EXPERT is an internet based, exploratory study to assess feasibility and measure the impact of online health information, (experiential and fact-based) for self-management of asthma, motivation to stop smoking, and preparedness for caring for someone with multiple sclerosis.• Responsibility for all aspects of trial management• Production of study protocol• Identified sites suitable for participation• Developed site monitoring plan and documentation• Arranged and attended… Show more EXPERT is an internet based, exploratory study to assess feasibility and measure the impact of online health information, (experiential and fact-based) for self-management of asthma, motivation to stop smoking, and preparedness for caring for someone with multiple sclerosis.• Responsibility for all aspects of trial management• Production of study protocol• Identified sites suitable for participation• Developed site monitoring plan and documentation• Arranged and attended site initiation visits • Designed electronic data capture and reporting systems • REC and R&D submissions• Design and implementation of recruitment strategies• Coordinated and chaired research team meetings• Produced and presented progress reports • Created and maintained the Trial Master File• Ensured compliance with ICH-GCP Show less

Aug 2012 - Feb 2014

Project & Data Manager, Acst-2

Oxford, United Kingdom

ACST-2 is an international, multi-centre, randomised trial comparing the surgical procedures carotid endarterectomy (CEA) with carotid artery stenting (CAS) in patients with carotid artery stenosis.• Responsibility for the day-to-day running of the trial• Line managed the Communications Manager and Study Coordinator• Facilitated the provision of online randomisation services• Developed data collection and reporting systems • Maintaining good communication with… Show more ACST-2 is an international, multi-centre, randomised trial comparing the surgical procedures carotid endarterectomy (CEA) with carotid artery stenting (CAS) in patients with carotid artery stenosis.• Responsibility for the day-to-day running of the trial• Line managed the Communications Manager and Study Coordinator• Facilitated the provision of online randomisation services• Developed data collection and reporting systems • Maintaining good communication with participating centres• Produced SOPs and guidance notes for trial procedures • Chaired and presented at project planning meetings • Promoted the study at international research conferences • Managed the collection, quality control and verification of study data• Produced and maintained systems for statistical reporting• Monitored recruitment figures, data quality and completeness and provided updates to participating centres, Data Monitoring Committee, Steering Committee and funding bodies as required• Maintained patient files and ensured patient data was current, correct and complete• Developed good working relationships with external departments • Ensured that the study was run in compliance with the protocol and all necessary approvals and permissions were obtained• Worked to the ICH Good Clinical Practice guidelines Show less

Dec 2010 - Aug 2012

Sr. Clinical Research Associate

Sgs
Mar 2015 - May 2015

Study Administrator, Heart Protection Study

Oxford, United Kingdom

The Heart Protection Study was a multi-centre, randomised, double-blinded, placebo-controlled trial testing the long-term benefits of a cholesterol lowering drug.• Design and maintenance of study database • Dealt promptly and effectively with enquiries from clinical staff involved and participating patients• Routinely ran data checking programs and resolved verification queries on patient data files• Distributed regular reports to nursing staff at national clinic… Show more The Heart Protection Study was a multi-centre, randomised, double-blinded, placebo-controlled trial testing the long-term benefits of a cholesterol lowering drug.• Design and maintenance of study database • Dealt promptly and effectively with enquiries from clinical staff involved and participating patients• Routinely ran data checking programs and resolved verification queries on patient data files• Distributed regular reports to nursing staff at national clinic centres• Processed documentation and dispatched medical supplies to patients and clinics• Dealt with referrals from nursing staff for patients to transfer to GP follow up • Processed blood test results and liaised with the lead clinician regarding follow up action Show less

Nov 1998 - Apr 2004

Study Administrator, Atlas

Oxford, United Kingdom

ATLAS was an international multi-centre, randomised drugs trial for breast cancer patients. • Maintenance of the study database • Monitored and maintained financial records of regional centres• Distributed papers, agendas and minutes for internal and external meetings• Designed and despatched regular progress reports to National Coordinators • Serviced the trial steering committee, organised meetings and distributed papers • Coordinated the translation and… Show more ATLAS was an international multi-centre, randomised drugs trial for breast cancer patients. • Maintenance of the study database • Monitored and maintained financial records of regional centres• Distributed papers, agendas and minutes for internal and external meetings• Designed and despatched regular progress reports to National Coordinators • Serviced the trial steering committee, organised meetings and distributed papers • Coordinated the translation and printing of study protocols, posters and information booklets • Promoted the study at international conferences • Produced a manual of Standard Operating Procedures Show less

Jul 1996 - Oct 1998

Data Manager

Oxford, United Kingdom

• Monitored and updated the patient database• Identified and corrected data discrepancies • Requested missing or overdue paperwork as appropriate • Produced and distributed study documentation• Coordinated large international mailings• Developed a working knowledge of Latex Publishing Package

Sep 1995 - Jun 1996
Team & coworkers

Colleagues at IQVIA

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3 education records

Ally Bradley education

Education record

Burford School, Oxfordshire
FAQ

Frequently asked questions about Ally Bradley

Quick answers generated from the profile data available on this page.

What company does Ally Bradley work for?

Ally Bradley works for IQVIA.

What is Ally Bradley's role at IQVIA?

Ally Bradley is listed as Project Manager - Software Solutions at IQVIA.

What is Ally Bradley's email address?

AeroLeads has found 1 work email signal at @nds.ox.ac.uk for Ally Bradley at IQVIA.

Where is Ally Bradley based?

Ally Bradley is based in Oxford, England, United Kingdom while working with IQVIA.

What companies has Ally Bradley worked for?

Ally Bradley has worked for Iqvia, Genesiscare, University Of Oxford, Sgs, and Ctsu, University Of Oxford.

Who are Ally Bradley's colleagues at IQVIA?

Ally Bradley's colleagues at IQVIA include Sajini S, Sarbani Chakrabarty, Elaheh Naeimi Rad, Mohamed El Gafy, and Jamie Corsiga.

How can I contact Ally Bradley?

You can use AeroLeads to view verified contact signals for Ally Bradley at IQVIA, including work email, phone, and LinkedIn data when available.

What schools did Ally Bradley attend?

Ally Bradley holds Materials Engineering from University Of Wales, Swansea.

What skills is Ally Bradley known for?

Ally Bradley is listed with skills including Clinical Trials, Data Management, Gcp, Clinical Research, Clinical Research Governance, Project Management, Site Set Up And Monitoring, and Production Of Sops.

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