84 Clinical Research Coordinator jobs in the United Kingdom
Clinical Research Coordinator
Posted 4 days ago
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Job Description
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.
Clinical Research Coordinator
Posted 23 days ago
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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 submit your CV or get in touch via email:
Clinical Research Coordinator
Posted 1 day ago
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Job Description
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
Clinical Research Coordinator - Oncology
Posted 1 day ago
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Job Description
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.
- 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.
Clinical Research Coordinator - Halifax, UK

Posted 13 days ago
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Job Description
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
Clinical Research Coordinator - Halifax, UK

Posted 13 days ago
Job Viewed
Job Description
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
Junior Associate Director - Healthcare Research
Posted today
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Job Description
£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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Insights Analyst – Healthcare Equity Research
Posted today
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Data Scientist – Healthcare Research
Increase your chances of an interview by reading the following overview of this role before making an application.Location: London (Hybrid: Office & Remote)
Compensation: Competitive performance-based bonus
About Us
We are a specialist healthcare equity research boutique, providing independent equity research to the world’s largest institutional investors. Our focus spans the global healthcare and CDMO sectors, where we leverage deep domain expertise and data-driven insights to generate differentiated, value-creating trading ideas. We are a small, highly focused team with decades of experience, a growing reputation and significant room for growth.
The Role
We are seeking an Insights Analyst to join our research team. This role is ideal for someone who thrives on uncovering new datasets, finding trends and using advanced analytics to generate insights that support high-quality equity research.
You will work closely with senior equity analysts to integrate data into our investment ideas and help drive the discovery of new narratives in healthcare equity markets. You will be given significant autonomy and intellectual freedom.
Responsibilities
- Identify and source new datasets relevant to healthcare and CDMO sectors
- Analyse and interpret existing data from sources such as Symphony (TRx/NRx), Visible Alpha, Bloomberg, EvaluatePharma, company filings, FDA/EMA databases and clinicaltrialsdotgov
- Develop tools to scrape, clean and automate data workflows
- Apply coding, statistical methods and AI techniques to identify patterns and actionable insights
- Support the equity research process by generating data-driven narratives that enhance investment ideas
- Collaborate with the research team while operating independently and proactively
Requirements
- Strong excel knowledge
- Coding and data manipulation skills (e.g. Python, R, SQL, or similar)
- Experience with data scraping, automation and workflow optimisation
- Ability to effectively leverage AI tools in data analysis
- Analytical mindset with a passion for identifying trends and narratives in complex datasets
- Independent, self-motivated and comfortable working in a small, fast-paced team environment
- Would be an advantage to have familiarity with financial/healthcare datasets (e.g. Bloomberg, EvaluatePharma, Symphony)
What We Offer
- Competitive compensation with performance-based bonus
- 25 days annual holiday (plus
Data Management Analyst
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
Data Management Intern
Posted 28 days ago
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Job Description
**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