28 Clinical Coordinator jobs in the United Kingdom
Clinical Coordinator
Posted 15 days ago
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Job Description
We have an excellent opportunity for an experienced Clinical Coordinator with excellent communication skills to join a busy team in the outskirts of Reading. This role is pivotal in providing a seamless experience for patients referred for advanced treatments, while also supporting the clinicians and administrative team with efficient and effective coordination.
- Job Type: 12 month fixed-term contract
- Location: Pangbourne
- Working Hours: Monday to Thursday 8AM - 5:15PM, Fridays 8AM - 4PM (Part time hours also considered)
- Salary: Dependent on experience
As the Clinical Coordinator, you will be responsible for:
- Act as the main point of contact for all incoming referrals.
- Liaise with dentists to collect all necessary clinical information.
- Ensuring patients are followed up, booked in and informed at every stage.
- Providing patients with treatment information, fee estimates and appointment options.
- Ensuring all documentations are prepared and distributed and maintain all patient records ensuring they are kept up to date with referrals and treatment progress.
- Provide exceptional patient care and customer service.
The successful Clinical Coordinator have the following related skills / experience:
- Previous clinical experience within a dental or healthcare setting would be highly beneficial but not essential.
- Exceptional organisational and administrative skills.
- Excellent written and verbal communication skills.
- Confident, professional and compassionate.
For more information, please contact Julie Harding or Chloe Bennett on (phone number removed)
Clinical Coordinator
Posted 1 day ago
Job Viewed
Job Description
We have an excellent opportunity for an experienced Clinical Coordinator with excellent communication skills to join a busy team in the outskirts of Reading. This role is pivotal in providing a seamless experience for patients referred for advanced treatments, while also supporting the clinicians and administrative team with efficient and effective coordination.
- Job Type: 12 month fixed-term contract
- Location: Pangbourne
- Working Hours: Monday to Thursday 8AM - 5:15PM, Fridays 8AM - 4PM (Part time hours also considered)
- Salary: Dependent on experience
As the Clinical Coordinator, you will be responsible for:
- Act as the main point of contact for all incoming referrals.
- Liaise with dentists to collect all necessary clinical information.
- Ensuring patients are followed up, booked in and informed at every stage.
- Providing patients with treatment information, fee estimates and appointment options.
- Ensuring all documentations are prepared and distributed and maintain all patient records ensuring they are kept up to date with referrals and treatment progress.
- Provide exceptional patient care and customer service.
The successful Clinical Coordinator have the following related skills / experience:
- Previous clinical experience within a dental or healthcare setting would be highly beneficial but not essential.
- Exceptional organisational and administrative skills.
- Excellent written and verbal communication skills.
- Confident, professional and compassionate.
For more information, please contact Julie Harding or Chloe Bennett on (phone number removed)
Clinical Project Coordinator
Posted 9 days ago
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Job Description
Clinical Project Coordinator
Job Type: Temporary
Location: London/Remote
Contract Length: 12 months
Rate: circa. 350 per day
SRG are collaborating with a global Pharmaceutical Company who have a new opening for a Clinical Project Coordinator to support the team for a 12 month contract. This role has been designed to be in support of the Clinical Development excellence team. This will include providing project management support such as planning and conducting meetings and ensuring operational tasks within the group are performed to regulatory and quality standards.
Main Responsibilities may include:
- Leads and/or facilitates activities to support project or process lead in the successful execution of the project/process
- Schedules and prepares project meetings and workshops according to meeting excellence (including logistics, agenda, minutes, action items)
- Handles inquiries from stakeholders as a first contact, monitors against deliverables of various stakeholders, flags issues, opportunities and solutions to project/process lead
- Captures and reports project/process metrics
- Maintains associated SharePoint sites, monitors needs to adapt content; independently drives agreement process with respective members and continuously updates
- Maintains network information, calendars & schedules, mailboxes, FAQ documentation
Skills/experience required:
- Bachelor or Master degree in science or business related studies
- Associate degree or equivalent required if accompanied by 2 years Drug Development experience
- Proven track record in project management skills
- Familiar with the Drug Development process
- Able to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude
- Ability to simplify processes while delivering on given objectives
- Strong analytical and data driven mind-set
- Action orientated mindset: make things happen - exhibit a strong will to drive change
- Ability to work independently without much direction and guidance
- Strong interpersonal, communication (written and verbal) and negotiation skills
To Apply:
If you want to find out more about this role or would like to make an application, please click to apply and/or email me: to discuss in more detail.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Clinical Project Coordinator
Posted 1 day ago
Job Viewed
Job Description
Clinical Project Coordinator
Job Type: Temporary
Location: London/Remote
Contract Length: 12 months
Rate: circa. 350 per day
SRG are collaborating with a global Pharmaceutical Company who have a new opening for a Clinical Project Coordinator to support the team for a 12 month contract. This role has been designed to be in support of the Clinical Development excellence team. This will include providing project management support such as planning and conducting meetings and ensuring operational tasks within the group are performed to regulatory and quality standards.
Main Responsibilities may include:
- Leads and/or facilitates activities to support project or process lead in the successful execution of the project/process
- Schedules and prepares project meetings and workshops according to meeting excellence (including logistics, agenda, minutes, action items)
- Handles inquiries from stakeholders as a first contact, monitors against deliverables of various stakeholders, flags issues, opportunities and solutions to project/process lead
- Captures and reports project/process metrics
- Maintains associated SharePoint sites, monitors needs to adapt content; independently drives agreement process with respective members and continuously updates
- Maintains network information, calendars & schedules, mailboxes, FAQ documentation
Skills/experience required:
- Bachelor or Master degree in science or business related studies
- Associate degree or equivalent required if accompanied by 2 years Drug Development experience
- Proven track record in project management skills
- Familiar with the Drug Development process
- Able to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude
- Ability to simplify processes while delivering on given objectives
- Strong analytical and data driven mind-set
- Action orientated mindset: make things happen - exhibit a strong will to drive change
- Ability to work independently without much direction and guidance
- Strong interpersonal, communication (written and verbal) and negotiation skills
To Apply:
If you want to find out more about this role or would like to make an application, please click to apply and/or email me: to discuss in more detail.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Clinical Discharge Coordinator
Posted 8 days ago
Job Viewed
Job Description
Ilarna is dedicated to improving patient flow and supporting hospitals to reduce delayed transfers of care, ensuring individuals receive personalised care packages that meet their needs.
About the Role
We are looking for a dedicated and compassionate Clinical Discharge Coordinator to support the safe and timely transition of patients from hospital to home. This role is central to Ilarna’s mission.
Responsibilities
Hospital Engagement
- Develop and maintain strong relationships with ward staff, discharge teams, social workers, and community services.
- Act as the primary clinical point of contact for discharge planning.
Clinical Assessment & Discharge Coordination
- Undertake clinical assessments to inform safe and appropriate discharge planning.
- Ensure that individual care needs are clearly identified and incorporated into tailored care packages.
Care Package Facilitation
- Work collaboratively with Ilarna’s care teams to allocate the right Personal Assistants and clinical support.
- Ensure that care packages are safe, compliant, and aligned with clinical recommendations.
Problem Solving & Escalation
- Anticipate and address potential barriers to discharge.
- Escalate complex clinical or operational issues to the Director of Care and wider leadership team when required.
Reporting & Documentation
- Maintain accurate clinical records of referrals, assessments, discharges, and care outcomes.
- Provide regular reporting to demonstrate patient flow improvements and service impact.
Stakeholder Collaboration
- Participate in multi-disciplinary team (MDT) meetings, ward rounds, and discharge forums.
- Build effective partnerships with NHS colleagues, community teams, and social care services.
Quality & Governance
- Ensure all discharges and care arrangements comply with CQC standards and clinical governance requirements.
- Contribute to continuous service improvement and best practice development.
Qualifications
- Registered healthcare professional (nurse, AHP or equivalent) with current registration.
- Experience of hospital discharge processes and community care pathways.
Required Skills
- Strong clinical assessment skills with the ability to make safe, evidence-based decisions.
- Excellent communication, influencing, and relationship-building skills.
- Ability to work in a fast-paced hospital environment while maintaining a person-centred approach.
- Strong organisational and problem-solving skills.
Preferred Skills
- Knowledge of CQC-regulated domiciliary care (desirable)
For more information about this role please apply or reach out to our Chief Partnerships Officer Sam Alsop-Hall
Clinical Research Coordinator
Posted 15 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 Study Coordinator
Posted 13 days ago
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Job Description
**Location:** Witney, Oxfordshire
**ABOUT OUR DIABETES CARE DIVISION:**
Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential - because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions - across the spectrum of health, around the world, for all stages of life. Whether it's next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.
World Leader in Glucose Monitoring, Abbott Diabetes Care designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings. We have a Centre of Excellence in Witney for the development and manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. The site has been instrumental in the research, development and manufacture of the FreeStyle Libre Flash Glucose Monitoring System as well as exciting developments in the Libre family including FreeStyle Libre 2, FreeStyle Libre 3 and the Libre Sense system. We are passionate about doing work that improves the quality of people's lives.
**THE OPPORTUNITY:**
Known for the development of revolutionary technologies, Abbott Diabetes Care (ADC) designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings. We are passionate about doing work that improves the quality of people's lives. We now have an exciting opportunity in our growing Clinical Affairs function for a Clinical Study Coordinator.
The Clinical Study Co-coordinator assists delivery of studies to support both product development, manufacturing and the post market surveillance program for all ADC products
**ABOUT YOU:**
In this role, you will typically find yourself supporting the Clinical Research Associates (CRAs) in their study activity. This covers various activities, including ensuring adequate stock levels of product; scheduling, prioritising and coordinating shipment of product to trial sites; decontaminating returned product; assisting in preparation and maintenance of documentation and files; and liaison with both internal and external stakeholders to ensure smooth running of trial activities.
To be successful, you will ideally be qualified to secondary level education, and have an interest in Science, Technology, and clinical trials. The ideal candidate will be a proactive individual who takes initiative and is able to work within a team. You will need to be organised, and have good communication and time management skills, and be comfortable working in a fast-paced, changing environment. There will be opportunity to collaborate with multiple teams across the Abbott Diabetes Care business, including Data Management, Regulatory, Statistics, and Scientific Affairs.
**WHAT WE OFFER:**
At Abbott, you will be part of a dynamic team that is making a real difference in diabetes care. You will have the opportunity to work on cutting-edge technology and contribute to innovative solutions that improve lives. We offer a collaborative work environment, opportunities for professional growth, and the chance to be part of a company that values scientific excellence and innovation.
In addition to a competitive salary, Abbott offers a highly attractive benefits package which includes a defined-contribution pension scheme, a share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme which you can tailor to your own requirements. We like to help our employee's live life to the fullest, and therefore we offer a range of optional initiatives for you to get involved in, including onsite allotments, couch to 5k campaigns, bee keeping, yoga and more!
**APPLY NOW:**
If you are passionate about electrochemistry and eager to contribute to ground-breaking research and development, we invite you to apply for this exciting opportunity. Join us in advancing diabetes care and making a positive impact on the world.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Clinical Research Coordinator
Posted today
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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 - Halifax, UK

Posted 5 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
Clinical Research Coordinator - Halifax, UK

Posted 5 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