Research operations occupations Work, Jobs in Burghfield, Brk (with Salaries)

Principal Clinical Data Standards Consultant
ICON Plc —Reading
- Full-time
- Remote
- Programmable logic controllers
- Bachelor's degree
- Mentoring
- Employee assistance programme
Research Assistant
West London NHS Trust —Crowthorne
- £36,943 - £44,900 a year
- Full-time
3d
Study Start Up Associate I
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
13h
Clinical Research Associate II
IQVIA —Reading
- No degree
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
NTR Senior Technical Sponsor
AWE —Reading
- From £47,860 a year
- Full-time
- Military
- Project management
- Free parking
- Annual leave
13d
Research and Development Manager
Infinitesima —Abingdon
- £52,275 - £77,987 a year
- Hybrid work
- Doctoral degree
- Engineering
- Master's degree
- Annual leave
Quick apply
13d
CRA base
ICON Plc —Reading
- Full-time
- Patient monitoring
- English
- Bachelor's degree
- Employee assistance programme
Biosamples Operations Specialist
UCB —Slough
- Microsoft Office
Clinical Project Manager I
Perspectum —Oxford
- £33,000 - £45,000 a year
- Full-time
- Project management
- Communication skills
Quick apply
Senior Clinical Trials Assistant
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
14d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £230,000 - £270,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
Feasibility Analyst
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Excel
- Analysis skills
- Presentation skills
- Employee assistance programme
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Project Manager
Theolytics —Oxford
- Organisational skills
- IT
- Communication skills
- Flexible schedule
Linguistic Validation & eCOA Team Lead
IQVIA —Reading
- Customer service
- Microsoft Office
- Bachelor's degree
Study Start Up Manager
ICON Plc —Reading
- Full-time
- Project management
- Communication skills
- Employee assistance programme
Head of Diagnostics and Data Controls (DDC)
Tokamak Energy —Abingdon
- £80,000 - £100,000 a year
- Full-time
- Hybrid work
- No degree
- Leadership
- Communication skills
Quick apply
12d
Patient Recruitment Lead
ICON Plc —Reading
- Full-time
- Analysis skills
- Bachelor's degree
- Communication skills
- Employee assistance programme

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research operations occupations jobs near burghfield, brk

Principal Clinical Data Standards Consultant

ICON Plc -
Reading

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Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Programmable logic controllers
Bachelor's degree
Data management
Mentoring
Leadership
Communication skills
FDA regulations

Full job description

Principal Data Standards Consultant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Principal Data Standard Consultant

As a Principal Clinical Data Standards Consultant at ICON Plc, you will:

Provide expert-level functional knowledge in at least one standards domain, contributing to the development of standards content both internally and for sponsor-facing projects.
Develop, implement, and maintain ICON Data Collection standards libraries in compliance with CDISC, sponsor, and regulatory requirements.
Act as a subject matter expert to guide standards implementation and ensure compliance across clinical data management activities.
Apply deep understanding of business challenges to recommend and drive best practices, improving processes, products, and services to enhance competitive differentiation.
Collaborate cross-functionally to define data collection strategies and standards for clinical trials.
Participate in standards governance activities, influencing decision-making and providing expert input on complex topics.
Lead or contribute to departmental initiatives, potentially acting as a project lead with responsibility for coordinating team members.
Support the development of training materials and reference documentation across standards topics such as CDASH & Controlled Terminology.
Stay up to date with industry trends, regulatory changes, and emerging standards, ensuring continuous improvement of ICON practices.
Provide mentorship and guidance to more junior team members.

Requirements:

A Bachelor’s degree in a relevant discipline (e.g., Life Sciences, Computer Science, or similar); advanced degrees are advantageous.
Approximately 8+ years of experience in clinical data management, with significant expertise in data standards.
Advanced proficiency in CDISC standards (CDASH, SDTM, Controlled Terminology, etc.) and strong knowledge of regulatory requirements (FDA, EMA, etc.).
Proven experience with EDC build/design tools, such as Medidata Rave and/or Veeva Vault EDC/CDMS.
Demonstrated ability to solve complex problems, using advanced analytical thinking and sound judgment to develop innovative solutions.
Strong leadership capabilities, including experience leading initiatives or mentoring team members.
Excellent interpersonal, communication, and influencing skills, with the ability to present, defend analyses, and secure stakeholder alignment on complex topics.
Ability to significantly impact operational, project, or departmental objectives, ensuring delivery of high-quality outcomes aligned with business strategy.

If you are ready to make a meaningful impact in the field of clinical data standards and contribute to innovative, high-impact clinical projects, we encourage you to apply and join ICON’s growing team.

#LI-JC3

#LI-Remote

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

Refine Your Search

research operations occupations jobs in burghfield, brk

Principal Clinical Data Standards Consultant

Research Assistant

Study Start Up Associate I

Clinical Research Associate II

Specialist, R&D Contracts & Business Operations

NTR Senior Technical Sponsor

Research and Development Manager

CRA base

Biosamples Operations Specialist

Clinical Project Manager I

Senior Clinical Trials Assistant

CRA

Director, Portfolio Development Process & Standards Lead

Feasibility Analyst

Clinical Research Associate

Project Manager

Linguistic Validation & eCOA Team Lead

Study Start Up Manager

Head of Diagnostics and Data Controls (DDC)

Patient Recruitment Lead

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