81 Nursing Research jobs in the United Kingdom
Clinical Research Nurse II
Posted 18 days ago
Job Viewed
Job Description
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Clinical Research Nurse for our Synexus Clinical Research site in Birmingham, United Kingdom
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. The Clinical Research Nurse conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.
**Key responsibilities for a Clinical Research Nurse are as follows:**
+ Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
+ Provides medical care to patients, always ensuring patient safety comes first.
+ Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
+ Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
+ Records all patient information and results from tests as per protocol on required forms.
+ Where required, may complete IP accountability logs and associated information.
+ Reports suspected non-compliance to relevant site staff.
+ Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
+ Promotes the company and builds a positive relationship with patients to ensure retention.
+ Attends site initiation meetings and all other relevant meetings to receive training on protocol.
+ May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
+ Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
+ Gathers and maintains source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
+ Adheres to company COP/SCOP.
+ May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
+ Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
+ Demonstrated ability to exercise discretion and sound judgement
+ Good decision-making, negotiation and influencing skills - Good communication skills and English fluency will be an advantage
+ Good organizational skills
+ Good proficiency in basic computer applications
+ Good interpersonal skills to work in a team environment
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Clinical Research Nurse II
Posted 18 days ago
Job Viewed
Job Description
**Environmental Conditions**
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Clinical Research Nurse for our Synexus Clinical Research site in Cardiff, United Kingdom
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. The Clinical Research Nurse conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.
**Key responsibilities for a Clinical Research Nurse are as follows:**
+ Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
+ Provides medical care to patients, always ensuring patient safety comes first.
+ Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
+ Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
+ Records all patient information and results from tests as per protocol on required forms.
+ Where required, may complete IP accountability logs and associated information.
+ Reports suspected non-compliance to relevant site staff.
+ Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
+ Promotes the company and builds a positive relationship with patients to ensure retention.
+ Attends site initiation meetings and all other relevant meetings to receive training on protocol.
+ May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
+ Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
+ Gathers and maintains source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
+ Adheres to company COP/SCOP.
+ May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
+ Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
+ Demonstrated ability to exercise discretion and sound judgement
+ Good decision-making, negotiation and influencing skills - Good communication skills and English fluency will be an advantage
+ Good organizational skills
+ Good proficiency in basic computer applications
+ Good interpersonal skills to work in a team environment
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Clinical Research Coordinator
Posted 9 days ago
Job Viewed
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 Physician
Posted 16 days ago
Job Viewed
Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Clinical Research Physician
Posted 16 days ago
Job Viewed
Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Clinical Research Physician
Posted 19 days ago
Job Viewed
Job Description
Clinical Research Physician
Posted 19 days ago
Job Viewed
Job Description
Job Title: Clinical Research Physician
Location: Liverpool, UK
Employment Type: Full-time
Reports To: Medical Director / Principal Investigator / Site Director
About the Role:
We are seeking a motivated and experienced Clinical Research Physician to join our dynamic clinical trials network in Liverpool . This is a patient-facing role where you will act as a Sub-Investigator or Principal Investigator across a range of Phase I–IV clinical studies in collaboration with global sponsors and CROs. You will play a pivotal role in delivering high-quality clinical research within a network of well-established trial sites.
Key Responsibilities:
- Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on assigned clinical trials.
- Provide medical oversight and ensure participant safety throughout the study lifecycle.
- Conduct study-related procedures including medical assessments, physical examinations, and AE/SAE evaluations.
- Review and assess eligibility criteria, informed consent documentation, and patient medical histories.
- Liaise with study sponsors, monitors (CRAs), ethics committees, and regulatory authorities as needed.
- Ensure GCP compliance and adherence to protocol, SOPs, and applicable regulations.
- Contribute to site feasibility, study start-up, and recruitment planning activities.
- Support medical input into recruitment materials and protocol reviews.
- Maintain accurate documentation in accordance with regulatory and sponsor expectations.
- Provide clinical leadership and guidance to site staff including nurses, coordinators, and administrative teams.
Essential Qualifications and Experience:
- Medical degree (MBBS, MBChB or equivalent) and full GMC registration .
- Minimum 1–2 years of experience in clinical research or clinical trials (preferably Phase II–IV).
- Knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent clinical judgment and ability to make sound medical decisions.
- Strong communication and interpersonal skills.
- Ability to work effectively within a multidisciplinary team.
Desirable:
- Experience acting as PI or Sub-I in commercial clinical trials.
- Background in general medicine, internal medicine, or a therapeutic area relevant to trials (e.g., vaccines, cardiology, respiratory, CNS).
- Interest in expanding research expertise and participating in multiple therapeutic areas.
- ALS/BLS certification (training can be provided).
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Clinical Research Physician
Posted today
Job Viewed
Job Description
Urgent Nursing Opportunity
The Client
The company have had 18% over the past 2 years and are using this to further fuel their mission of connecting patients to clinical trials through their recruitment and retention activities. Founded by industry experts, they are using digital technologies to improve the reach and accessibility of clinical trials.
The Role
The role we have is for a Research Physician to support their ongoing clinical trial work dedicated to one of their site in either York or Preston.
Requirements
Minimum 4 years of experience in the NHS (Registrar level) - Making independent decisions on the ward, running outpatients clinics.
- GMC registered
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Clinical Research Associate
Posted today
Job Viewed
Job Description
Are you a passionate CRA II or Senior CRA looking for your next challenge?
We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusively with a leading Pharmaceutical client.
This is a unique opportunity to be part of a dynamic and supportive environment where your contributions directly impact the future of medicine. Our clients FSP model provides the stability and support of a dedicated team, while you gain exposure to the innovative research of a top-tier pharmaceutical company.
About the role:
As a CRA II or Senior CRA, you will be responsible for the full range of monitoring activities, from site initiation to close-out. You'll ensure the highest standards of data quality and compliance with ICH-GCP, protocols, and all applicable regulations. This role is home-based and will involve travel to sites across your designated region.
What our client offer:
- Salary: £45,000 - £55,000 per annum, depending on experience.
- Car/Car Allowance: A company car or a competitive car allowance.
- Bonus & Benefits: An attractive bonus scheme and a comprehensive benefits package.
- Career Growth: We are committed to your professional development and offer extensive training, mentorship, and opportunities for progression within our growing FSP.
Location:
This is a home-based role to be based in one of the following regions:
- North England
- North West England
- Midlands
- London
- South England
Requirements:
- Proven experience as a CRA, with a strong understanding of the clinical trial lifecycle. 18 months minimum as a CRA to be CRAII and 3 year + to be considered for Senior CRA.
- Excellent knowledge of ICH-GCP guidelines and relevant regulations.
- Strong communication and interpersonal skills.
- A proactive and independent approach to your work.
- A full UK driving licence and willingness to travel.
If you are ready to take the next step in your career and join a company that values growth, training, and support, we want to hear from you.
Apply now or message us for more details!
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