80 Clinical Research Coordinator jobs in the United Kingdom

Clinical Research Coordinator

Milton Keynes, South East Actalent

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Job Description

Job Title: Clinical Research Coordinator (Band 6 Nurse)

Contract Type: part time (2-3 days/week)

Overview:

We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.

Key Responsibilities:

  • Identify and recruit eligible patients for clinical trials.
  • Perform accurate and timely data entry into study databases.
  • Collaborate with research and clinical teams to ensure protocol compliance.
  • Maintain high standards of documentation and regulatory adherence.

Requirements:

  • Registered Band 6 Nurse with relevant clinical experience .
  • Demonstrated experience in patient identification and data entry.
  • Strong attention to detail and organizational skills.
  • Must be available to work every Wednesday, plus two additional weekdays.

Please get in touch to find out more.

Job Title: Clinical Research Coordinator

Location: Milton Keynes, UK

Job Type: Contract

Trading as Aerotek. Allegis Group Limited, Maxis 2, Western Road, Bracknell, RG12 1RT, United Kingdom. No Allegis Group Limited operates as an Employment Business and Employment Agency as set out in the Conduct of Employment Agencies and Employment Businesses Regulations 2003. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, Talentis Solutions, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice.

To access our Online Privacy Notice, which explains what information we may collect, use, share, and store about you, and describes your rights and choices about this, please go to the website.

We are part of a global network of companies and as a result, the personal data you provide will be shared within Allegis Group and transferred and processed outside the UK, Switzerland and European Economic Area subject to the protections described in the Allegis Group Online Privacy Notice. We store personal data in the UK, EEA, Switzerland and the USA. If you would like to exercise your privacy rights, please visit the "Contacting Us" section of our Online Privacy Notice for details on how to contact us. To protect your privacy and security, we may take steps to verify your identity, such as a password and user ID if there is an

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Clinical Research Coordinator

Milton Keynes, South East Actalent

Posted 3 days ago

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We're Hiring: Clinical Nurse

Focus Area: Multiple Myeloma Research

Are you a Band 6 Nurse with a keen eye for detail and a passion for clinical research? We're looking for someone to join our team at Milton Keynes University Hospital on a part-time basis (2–3 days/week) to support a research study in Multiple Myeloma .


What you'll be doing:

  • Patient identification and recruitment
  • Accurate clinical data entry
  • Supporting research operations on-site


What we're looking for:

  • NMC-registered Band 6 Nurse
  • Experience with patient identification and clinical data entry
  • Availability on Wednesdays , plus two additional weekdays
  • Strong communication and organisational skills
  • This is a great opportunity to contribute to impactful research while maintaining a flexible schedule.
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Clinical Research Coordinator

Milton Keynes, South East Actalent

Posted 22 days ago

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Job Title: Clinical Research Coordinator (Band 6 Nurse)

Contract Type: Part-Time (2–3 days/week)

Overview:

We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.


Key Responsibilities:

  • Identify and recruit eligible patients for clinical trials.
  • Perform accurate and timely data entry into study databases.
  • Collaborate with research and clinical teams to ensure protocol compliance.
  • Maintain high standards of documentation and regulatory adherence.


Requirements:

  • Registered Band 6 Nurse with relevant clinical experience.
  • Demonstrated experience in patient identification and data entry.
  • Strong attention to detail and organizational skills.
  • Must be available to work every Wednesday, plus two additional weekdays.


Please submit your CV or get in touch via email:

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Clinical Research Coordinator

Bath, South West Actalent

Posted 1 day ago

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URGENT HIRING: Clinical Research Coordinator – Bath

I'm reaching out with an exciting full-time opportunity for a Clinical Research Coordinator (CRC) to join a global clinical research service provider supporting multiple sponsors.

Therapeutic Area: Atopic Dermatitis (experience required)

Location: On-site in Bath

Start Date: ASAP

Duration: Until October (potential to extend)

This role is ideal for a Band 5/6 Nurse or Clinical Research Nurse ready to step into a CRC title.

Key Responsibilities:

  • Patient identification & chart reviews
  • Referral physician networking
  • Community outreach

Preferred Experience:

  • Background in nursing or clinical research
  • Familiarity with Millennium Sauna or other EDC systems
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Clinical Research Coordinator - Oncology

SO14 0AA Southampton, South East £30000 Annually WhatJobs

Posted today

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full-time
Our client is seeking a meticulous and organized Clinical Research Coordinator to support critical oncology research studies in **Southampton, Hampshire, UK**. This role is fundamental to the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for a range of activities, including patient recruitment and screening, informed consent process, data collection and entry, and study documentation management. This involves working closely with principal investigators, research nurses, and study sponsors to facilitate the smooth progression of clinical trials. Key duties include scheduling patient visits, managing study supplies, and ensuring accurate and timely completion of case report forms (CRFs) and other study-related documents. You will also play a vital role in monitoring patient compliance and safety, reporting any adverse events promptly. The ideal candidate will have a strong understanding of clinical trial processes, GCP (Good Clinical Practice) guidelines, and regulatory requirements. Excellent organizational skills, meticulous attention to detail, and proficiency in data management software are essential. Strong interpersonal and communication skills are required to interact effectively with patients, healthcare professionals, and study teams. Previous experience in clinical research, particularly in oncology, is highly desirable. A background in nursing, life sciences, or a related field would be beneficial. Join our client to contribute to advancing cancer treatments through impactful research.

Key Responsibilities:
  • Coordinate the conduct of clinical trials according to study protocols and GCP guidelines.
  • Screen potential participants for eligibility and manage the informed consent process.
  • Schedule patient appointments and manage study-related visits.
  • Collect, manage, and accurately enter clinical data into study databases.
  • Maintain all study-related documentation and regulatory files.
  • Monitor patient adherence to the study protocol and report any deviations.
  • Record and report adverse events and serious adverse events promptly.
  • Liaise with investigators, research staff, and study sponsors.
  • Manage study supplies and equipment.
  • Ensure compliance with all applicable regulatory requirements.
Required Qualifications:
  • Bachelor's degree in Nursing, Life Sciences, or a related field.
  • Proven experience as a Clinical Research Coordinator or in a similar role.
  • Thorough understanding of clinical trial phases, GCP, and regulatory requirements.
  • Excellent organizational and time management skills.
  • Meticulous attention to detail in data collection and documentation.
  • Strong interpersonal and communication skills, with the ability to interact with patients and professionals.
  • Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
  • Ability to work independently and as part of a multidisciplinary team.
  • Knowledge of oncology clinical research is a significant advantage.
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Clinical Research Coordinator - Halifax, UK

Leeds, Yorkshire and the Humber IQVIA

Posted 12 days ago

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Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.
This part-time role is to support a site in **Halifax, West Yorkshire** in conducting a clinical trial for 15 hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
**Day to day responsibilities will include:**
+ Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
+ Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns
+ Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Plan and coordinate logistical activity for study procedures according to the study protocol
+ Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
+ Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
+ Correct custody of study drug according to site standard operating procedures
+ Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
**We are looking for candidates with the following skills and experience:**
+ BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
+ Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
+ Good organizational skills with the ability to pay close attention to detail.
#LI-DNP
#LI-HCPN
#LI-CES
#LI-CT1
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 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
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Clinical Research Coordinator - Halifax, UK

Halifax, Yorkshire and the Humber IQVIA

Posted 12 days ago

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Job Description

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.
This part-time role is to support a site in **Halifax, West Yorkshire** in conducting a clinical trial for 15 hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
**Day to day responsibilities will include:**
+ Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
+ Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns
+ Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Plan and coordinate logistical activity for study procedures according to the study protocol
+ Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
+ Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
+ Correct custody of study drug according to site standard operating procedures
+ Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
**We are looking for candidates with the following skills and experience:**
+ BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
+ Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
+ Good organizational skills with the ability to pay close attention to detail.
#LI-DNP
#LI-HCPN
#LI-CES
#LI-CT1
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 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
This advertiser has chosen not to accept applicants from your region.

Junior Associate Director - Healthcare Research

London, London Harnham

Posted 1 day ago

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Junior Associate Director - Healthcare Research

£55,000-£60,000 | Remote (UK or Germany-based)
Build, lead, and influence - without red tape

A small-but-mighty healthcare insights agency is looking for a strategic, commercially-minded Junior AD to help scale their offering. If you're looking for impact, autonomy, and a break from corporate hierarchy - let's talk.

THE COMPANY
This is a nimble, full-service agency with a European footprint, recently re-energised under new leadership. They're growing fast, with a focus on pharma and biotech clients, and want someone who can bring fresh thinking to their approach.

THE ROLE
You'll step in as a player-coach, driving projects while influencing the shape of the team and proposition. Expect high-impact work, limited bureaucracy, and big visibility.

  • Leading end-to-end international quant projects

  • Shaping proposals, pitches, and client strategy

  • Managing researchers and mentoring mid-level talent

  • Contributing to innovation and internal process improvement

  • Collaborating with UK and German teams (language skills a bonus)

YOU'LL NEED

  • Strong quant experience within healthcare market research

  • Confident running global studies and managing client relationships

  • A strategic mindset with hands-on execution skills

  • Ready to take ownership and lead from the front

  • Based in the UK or Germany

WHY APPLY?

  • Work in a collaborative, remote-first environment

  • Chance to shape internal research innovation (think AI, automation, modernisation)

  • High exposure to leadership and business development

  • Unique access to an in-house physician panel

  • Rapid progression and clear career path

INTERVIEW PROCESS

  • Intro chat with senior leadership

  • Task/presentation stage

  • Final meet-the-team session (if needed)

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Data Management Analyst

Warrington, North West SF Technology Solutions

Posted 1 day ago

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Data Governance Analyst

£50,000 + benefits

Hybrid – 2 days per week onsite (North West)


We’re working with a well-established organisation in the healthcare sector that is investing in its data capability and building out its data governance approach from the ground up.


This is a newly created role for someone who’s ready to own data governance across the business not from a distance, but by getting hands-on, engaging stakeholders, and helping teams make better decisions with more trustworthy data.


You’ll work closely with the Head of Data & Analytics and colleagues across operations, finance, and supply chain to embed governance into day-to-day processes and define what good looks like.


What you’ll be doing:

  • Map out current data usage, identify ownership gaps, and propose practical solutions
  • Define and embed data ownership, stewardship roles, and business glossaries
  • Support the improvement of data quality through guidance, documentation, and collaboration
  • Help teams adopt consistent definitions, fix duplication and inconsistency issues
  • Provide clear, accessible governance documentation and be a go-to resource for stakeholders
  • Engage widely across the business to build trust, increase adoption, and embed data accountability


What we’re looking for:

  • Hands-on experience with data governance, data quality, or data stewardship (e.g. from an analyst, data coordinator, or governance role)
  • Strong communication and relationship-building skills – someone confident engaging with stakeholders and helping them understand the value of governance
  • A mindset that balances structure with flexibility – this isn’t a policy-heavy role, it’s about getting things done
  • Any experience with Power BI, SQL, or Microsoft Purview is helpful, but not essential


Why apply?

  • You’ll have ownership of the governance agenda, with backing from senior leadership
  • It’s a chance to shape data practices in a business that wants to modernise how it uses information
  • Hybrid working – with 2 days a week onsite in the North West
  • A practical, hands-on role where your communication skills are just as important as your data knowledge
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Data Management Intern

Westerham, South East Bombardier

Posted 27 days ago

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Bombardier's Business Aircraft London Service Centre in Biggin Hill is part of an award-winning network and is the flagship of Bombardier's European operation. This Base and Line Maintenance Centre is the fastest-growing Service Centre in Europe and the largest Business Aircraft OEM in the UK. The facility has the capabilities to perform an array of maintenance checks, modifications and upgrades all from this site. Only 14 miles from London, Bombardier's Biggin Hill Service Centre is ideally located to support operators in the UK region and beyond.
**What are your contributions to the team?**
- Collect, clean, and validate maintenance scheduling data from various sources.
- Maintain and update aircraft maintenance schedules in internal systems.
- Track aircraft maintenance milestones and flag potential scheduling conflicts or delays.
- Support the integration of data from maintenance management systems into scheduling tools.
- Maintain accurate records of aircraft downtime, hangar occupancy, and technician availability.
- Participate in daily scheduling meetings and document action items related to data updates.
- Assist in creating dashboards and reports to monitor progress, resource utilization, and turnaround times.
- Contribute to the development and testing of automated tools or scripts to streamline data entry and reporting.
- Prepare compliance reports and audit documentation related to maintenance scheduling.
- Monitor and report on key performance indicators (KPIs) such as turnaround time, schedule adherence, and resource utilization.
- Collaborate with IT or data teams to troubleshoot data access or integrity issues.
- Archive and retrieve historical maintenance and scheduling data for analysis and forecasting.
- Ensure data privacy and security protocols are followed in line with company and regulatory standards.
- Help document data management processes and suggest improvements for efficiency and accuracy
**How to thrive in this role?**
- Able to work on site from Monday - Friday (40 hours per week)
- Strong proficiency in Excel; familiarity with Power BI is a plus.
- Excellent attention to detail and organizational skills.
- Strong analytical and problem-solving abilities.
- Good communication skills and ability to work in a team-oriented environment.
- Interest in aviation or aircraft maintenance is desirable but not essential.
Bombardier is an equal opportunity employer and encourages persons of any race, religion, ethnicity, gender identity, sexual orientation, age immigration status, disability or other applicable legally protected Characteristics to apply.
Whether your candidacy is moving on to the next step of the hiring process or not, we will keep you informed by email or by phone.
Join us at ideas move people.
**Job** Data Management Intern
**Primary Location** Biggin Hill Service Center
**Organization** Bombardier Services (UK)
**Employee Status**
**Requisition** 8624 Data Management Intern
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Senior Data Management Professional - Data Science - Data Management Lab

London, London Bloomberg

Posted 4 days ago

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Job Description

Senior Data Management Professional - Data Science - Data Management Lab





Location





London





Business Area





Data





Ref #










**Description & Requirements**



Bloomberg runs on data, and in the Data department we're responsible for acquiring, interpreting and supplying data insights to our clients. Our Data teams work to collect, analyse, process, and publish the data which is the backbone of our iconic Bloomberg Terminal -- the data which ultimately moves the financial markets! Weu2019re responsible for delivering this data, news, and analytics through innovative technology -- quickly and accurately.



The Data Management Lab (DML) sits within the Data organization, supporting Datau2019s pursuit of data management excellence by aligning industry best practices with Bloomberg's established expertise in financial market data. DML empowers our data professionals to make their products u201cready-to-useu201d by promoting increased data discoverability, accessibility, appraisability, interoperability, and analysis-readiness.



As a Data Management Professional, you will play a pivotal role in ensuring the delivery of high-quality data to our clients while driving impactful business decisions. You will be an integral member of a collaborative set of teams, Quality Methods & Insights under DML that includes Data Quality, Business Intelligence and Process Engineering serving as a centre of excellence for the rest of the teams in the Data organisation. A key aspect of this role involves leading initiatives to appraise and enhance the quality of our datasets, partnering closely with Data product and Engineering teams to champion effective solutions. Simultaneously, you will leverage your analytical expertise to support the development of scalable methods and tools for analysing product, process, and people data. The analytical insights will directly support data-driven decision-making aimed at achieving quality enhancements and process optimisation across the organization. You will also contribute to the ongoing refinement of data management best practices.



**As a valued member of our team, weu2019ll trust you to:**


Lead global initiatives focused on data science applications within the realms of data quality, data product development, and operational efficiency
Design and run studies to uncover root causes of data quality issues, using techniques such as hypothesis testing, clustering, and regression analysis
Develop statistical models to detect data anomalies, predict quality issues, and optimize data manufacturing pipelines by leveraging appropriate methodologies
Deliver actionable insights through advanced analytics, and compelling data storytelling to support business decision making and innovation
Collaborate with data stakeholders and engineering partner to translate high-impact questions into scalable data science solutions
Build statistical and analytical capabilities within the team; mentor others in applying best practices in modelling and experimentation



**Youu2019ll need to have a strong combination of the following:**



_*Please note we use years of experience as a guide but we certainly will consider applications from all candidates who are able to demonstrate the skills necessary for the role._


A PhD or Master's degree in Data Science, Economics, Statistics or a related quantitative field
3+ years' experience designing research studies as well as performing analysis such as data profiling, predictive modelling, and causal analysis
Strong coding skills ideally in Python and experience with SQL for data querying
Familiarity with version control systems (e.g., Git) and a collaborative development workflow (e.g., GitHub, GitLab)
Experience working in a data quality, data governance, or data management environment is a major plus (knowledge of DAMA, DCAM, etc. is welcome)
Excellent project management skills and the ability to communicate complex findings clearly to both technical and non-technical audiences
Knowledge of financial markets and Bloomberg products is a plus



**Does this sound like you?**



Apply if you think we're a good match. We'll get in touch to let you know what the next steps are.

Bloomberg is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of age, ancestry, color, gender identity or expression, genetic predisposition or carrier status, marital status, national or ethnic origin, race, religion or belief, sex, sexual orientation, sexual and other reproductive health decisions, parental or caring status, physical or mental disability, pregnancy or parental leave, protected veteran status, status as a victim of domestic violence, or any other classification protected by applicable law.

Bloomberg is a disability inclusive employer. Please let us know if you require any reasonable adjustments to be made for the recruitment process. If you would prefer to discuss this confidentially, please email
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