161 Medical Research jobs in the United Kingdom
Data Analyst - Healthcare Research
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Job Description
The NIHR are looking for a skilled and motivated Data Analyst to join our Data and Insights team, providing high-quality analytical support to both internal teams and external customers.
About Us
The National Institute for Health and Care Research (NIHR), funded by the Department of Health and Social Care, partners with the NHS, academia, local government, and the public to fund, enable, and deliver world-leading health and social care research, improving lives, driving innovation, and fostering global health impact.
Job Description
Join our Data and Insights team and play a key role in turning information into impact. Reporting to the Data Analytics Lead, you’ll work with talented analysts and a data engineer to keep our databases running smoothly, develop and improve QlikView dashboards, and create innovative solutions that meet evolving business needs. From answering high profile information requests to collaborating with colleagues across the NIHR and the Department of Health and Social Care, every day will bring variety and purpose. If you’re skilled in SQL, Excel/Google Sheets, and dashboarding tools like Qlik and you thrive on problem-solving and process improvement, we’d love to hear from you.
Key Responsibilities:
- Responding to information requests under tight KPIs, ensuring results match criteria
- Coding NIHR research to HRCS Health Categories and Research Activity Codes
- Producing analytical support for quarterly and annual reports
- Creating clear, engaging visualisations for stakeholder reports
- Designing dashboards in Qlik and developing Alteryx workflows to improve processes
- Managing and optimising large datasets in SQL Server Management Studio
- Enhancing SQL jobs, stored procedures, and troubleshooting performance issues
- Maintaining quality assurance standards and documentation
- Building strong working relationships and driving continuous improvement in data products and services
About You
Essential Criteria
- Degree in biomedical sciences, life sciences, or a related scientific discipline
- Minimum of 2 years’ experience in a data analyst or similar analytical role
- Previous experience or a strong interest in clinical research
- Advanced working knowledge of Alteryx, including development of complex workflows, use of macros, and integration with APIs
- Proficiency in Business Intelligence/Data Visualisation tools, preferably Qlik
- Expert-level skills in Microsoft Excel, with strong proficiency across Microsoft Office applications
Desired Criteria
- Understanding of the UKCRC Health Research Classification System (HRCS).
- An understanding of the research NIHR funds and supports.
- Familiar with various file-managements systems such as MS Sharepoint and Google Drive.
- Knowledge of SQL Server Integration Services (SSIS)
- Knowledge of SQL Server Reporting Services (SSRS)
- Knowledge of cloud hosted database environments such as Amazon Web Services or Google Cloud Platform
Position Details:
Salary: £40,300 per year
Location: Twickenham / Hybrid working model
Contract Type: Full Time, 12 month FTC - Secondment
Working Hours: 7.5 hours per day
Annual Leave: 25 days, plus UK public holidays
Employee Benefits Include:
Annual Bonus, subject to company performance
Enhanced Contributory Pension Scheme
Life Insurance Cover
Benenden Healthcare Membership
Training & Development Opportunities
Season Ticket Loan
Please note: This is an office based hybrid position, with a mandatory requirement to attend our office in Twickenham, London, one day each week.
NB: Interviews to commence from the 1st September.
Application
If you are excited about the prospect of joining our team and believe you possess the relevant skills and background, we invite you to apply. Please submit your CV along with a 'Statement of Suitability' that showcases your key skills and experiences in relation to the 'Required Criteria' outlined in the job description. Additionally, share your enthusiasm for working with NIHR.
Our Commitment to Equality and Diversity
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
Junior Associate Director - Healthcare Research
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£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)
Clinical Research Coordinator
Posted 5 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 Physician
Posted 11 days ago
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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 11 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 14 days ago
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Job Description
Clinical Research Physician
Posted 14 days ago
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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 Associate
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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!
#CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global
Clinical Research Physician
Posted today
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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
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Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)
Location: Hybrid UK Based
Employment Type: Freelance
Function: Clinical Operations
Therapeutic Area: Oncology
Reports To: Clinical Operations Manager
About the Role
We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.
Key Responsibilities
- Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
- Assist in site selection and feasibility assessments.
- Ensure proper documentation and timely resolution of site issues.
- Support site staff in understanding and complying with study protocols and GCP guidelines.
- Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
- Ensure timely collection and review of essential regulatory documents.
- Track patient recruitment and retention efforts at assigned sites.
- Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
- Maintain high-quality communication with clinical sites and sponsor/CRO teams.
- Escalate site performance or compliance issues as needed.
Required Qualifications
- Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
- Exposure to oncology trials (academic, site, or CRO experience).
- Understanding of ICH-GCP guidelines and regulatory requirements.
- Strong organizational skills with attention to detail.
- Ability to manage multiple tasks and priorities independently.
- Excellent communication and interpersonal skills.
- Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.