531 Clinical Trial Management jobs in the United Kingdom
Research Management System (RMS) Implementation Specialist, EMEA - Financial Solutions
Posted 6 days ago
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Job Description
Location
London
Business Area
Sales and Client Service
Ref #
**Description & Requirements**
The Bloomberg Financial Solutions department of 5,000+ employees is at the forefront of ensuring success for our customers and employees alike. Our team comprises several key pillars: Sales, Service, Operations, Culture and Brand. As a department, we are united by a common goal: We create meaningful relationships with clients by understanding their needs and delivering exceptional end-to-end support from sales and implementation, through their ongoing relationship with Bloomberg.
**Bloomberg's Research Management System (RMS)** is a fully integrated Buy-Side solution that empowers clients to manage investment research efficiently, compliantly, and collaboratively. Leveraging AI and Natural Language Processing (NLP), RMS enables clients to uncover insights across one of the world's largest libraries of broker research, company filings, transcripts, and internal notes. With seamless integration into Microsoft Office®, structured publishing workflows, and real-time collaboration tools, RMS centralizes qualitative and quantitative research, supports ESG engagement tracking, and connects to Bloomberg Query Language (BQL) for powerful analytics.
Our goal is to provide the most scalable research platform in the market - one that helps clients generate actionable ideas, manage compliance risk, and collaborate more effectively across the investment lifecycle.
**What is the role?**
The RMS Implementation Specialist plays a vital role in ensuring successful client engagements by combining deep product expertise with buy-side industry knowledge. You will partner with clients to analyze research workflows, configure RMS, deliver training, and ensure smooth integrations with portfolio management, compliance, and operational systems.
Unlike a generalist project manager, the Implementation Specialist is a hands-on product expert, guiding clients in how to best leverage RMS's AI-powered document search, collaboration, publishing, and ESG management features. You will own technical configurations, advise on workflow optimization, and champion best practices to maximize client adoption.
The role is based in London and covers new clients across EMEA, with some international travel required for on-site support.
**We'll trust you to:**
+ Lead RMS implementations from discovery to go-live, ensuring clients achieve business and workflow objectives.
+ Translate client requirements into tailored RMS configurations, including publishing workflows, data integrations, and compliance controls.
+ Guide clients on adopting AI/NLP-powered document search, BQL analytics, and ESG engagement management.
+ Deliver engaging training sessions for analysts, portfolio managers, and compliance teams.
+ Act as a product specialist during implementation, advising clients on maximizing collaboration tools, document annotation, and workflow automation.
+ Partner with Sales on scoping and solution design to ensure seamless handoff into implementation.
+ Manage multiple implementations concurrently, balancing project timelines and stakeholder expectations.
+ Provide structured feedback from client experiences to Product and Engineering to support ongoing innovation.
+ Drive adoption post-launch by monitoring usage, identifying opportunities for expansion, and embedding RMS into client workflows.
**You'll need to have:**
+ At least 4 years of financial technology implementation experience, ideally in Buy-Side research.
+ Strong expertise in investment research workflows, compliance oversight, and data-driven analytics
+ Excellent project management and project scoping abilities, with a track record of leading complex, multi-stakeholder implementations
+ Demonstrated ability to configure and implement enterprise platforms with technical integrations
+ Excellent client-facing skills: communication, training, and relationship management
+ A proactive, team-oriented approach with proven ability to work across multiple internal teams and departments such as Sales, Product and Engineering.
+ Critical thinking, problem-solving, and consultative skills with a proactive, client-first mindset
+ Strong Microsoft Office knowledge (Word, Excel, PowerPoint, Project, Visio)
**We would love to see:**
+ Prior experience working with AI/NLP solutions, publishing platforms, or data analytics tools.
+ Familiarity with Bloomberg applications; knowledge of AIM and/or PORT.
+ Experience with API-driven workflows.
+ Familiarity with programming languages (e.g. Python, Java).
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
Clinical Research Associate/ Senior Clinical Research Associate
Posted 1 day ago
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Job Description
About the Company
A fast-growing, tech-enabled CRO and global site network that started life within a major biopharma before becoming fully independent. They’ve built a proprietary AI platform now used to run smarter, faster clinical trials — and are expanding rapidly with their own hospitals and trial sites in India, and plans for Brazil, Australia, and China.
Now ~50 people, they’re closing Series A and moving into a Series B raise with a major bio-capital investor already signed. 0
It’s a genuine startup culture — everyone contributes, collaborates, and grows together. They also offer stock options from CRA level up – showing they invest in their people.
As their first UK CRA hire , you’ll have a key role in their European growth. You’ll monitor sites across the UK and EU (Spain, Greece, Italy, France, Germany) , support feasibility/start-up, and help shape the company’s operational foundations.
You’ll thrive here if you:
- Enjoy working autonomously in a small, fast-moving CRO.
- Want to help build something, not just follow a process.
- Can balance hands-on site work with cross-functional input.
What You’ll Need:
- 3 - 5 years CRA experience (CRO or sponsor)
- 5 - 7 years for a Senior CRA
- Proven EU monitoring exposure
- Solid knowledge of ICH-GCP & EU regs
- UK base with willingness to travel
- Startup or small-CRO experience is a big plus
- Oncology Based Experience
What’s on Offer:
- Competitive salary with higher flexibility for Senior CRA's
- Fast-track growth in a scaling, global business
- Exposure to AI-driven clinical operations
- Collaborative culture with true ownership and visibility
Clinical Research Physician
Posted 1 day ago
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Job Description
Planet Pharma are partnered with a leading clinical research organisation, who are seeking an experienced Research Physician with a strong clinical background and the ability to make independent decisions in a research environment.
Requirements:
- Minimum of 4 years’ experience in the NHS at Registrar level, including independent decision-making on the ward and running outpatient clinics.
- Background in General Medicine / Acute Internal Medicine.
- MRCP qualification.
- GMC registered – candidates must provide their GMC number.
- Right to work in the UK.
- Experience or exposure to clinical trials would be highly advantageous.
Candidates must be proactive, clinically competent, and ready to contribute to high-quality research delivery.
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
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 recognized 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 Coordinator
Posted 1 day ago
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Job Description
Join IQVIA as a Clinical Research Coordinator!
Are you passionate about clinical research and ready to make a real impact? Do you want to be part of a global leader in healthcare innovation? If so, we’d love to hear from you!
IQVIA is seeking a dedicated Clinical Research Coordinator to join our team in Torpoint , working 24 hours per week on a one year contract . This is a fantastic opportunity to contribute to cutting-edge clinical trials at a single site, supporting investigators and ensuring smooth study operations.
What You’ll Be Doing:
As a key member of the site team, you’ll play a vital role in supporting clinical research activities. Your responsibilities will include:
- Supporting clinical studies in line with health and safety policies under the guidance of the Principal Investigator.
- Maintaining study documentation including protocols, CRFs, and EDC systems.
- Coordinating logistics for study schedules.
- Assisting with data entry, quality checks, and resolving queries to ensure accuracy.
- Supporting patient recruitment and eligibility screening.
What We’re Looking For:
We’re seeking someone who is proactive, detail-oriented, and passionate about clinical research. Ideally, you’ll bring:
- At least 2 years’ experience as a Clinical Research Coordinator, Research Nurse, or Site Research Assistant.
- Solid understanding of clinical trials and study-specific procedures.
- Basic knowledge of medical terminology.
- Strong IT skills, including MS Office (Access, Outlook, Excel, Word).
- Excellent interpersonal and communication skills.
- Strong organisational abilities and attention to detail.
Why IQVIA?
At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research.
Clinical Research Physician
Posted 1 day ago
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Job Description
Exciting roles in cutting edge research, working with some of the most distinguished pharma companies in the UK and internationally
We’re offering
A rewarding career pathway for GMC registered physicians to become involved in the development of tomorrow’s medicines, in MHRA Phase I Accredited Unit with an international reputation.
The role
You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders.
Key responsibilities
To provide medical care and oversight of clinical trial participants.
To fulfil role of sub investigator/ Principal investigator when delegated ensuring compliance with regulatory and ethical standards.
A critical role in the design, execution and oversight of clinical trials.
To provide support to clinical staff and all other department in study set up and execution of clinical trials.
Working under the supervision of Professor Dave Singh, Medical Director. Applicants must have completed foundation year programme training or equivalent.
MEU will offer you.
· Competitive salary (dependant on experience)
· Continuous professional development
· 29 days annual leave increasing to 33 after 5 years' service
· Company pension scheme
· Generous annual bonus
· Healthcare plan
· Free parking
Clinical Research Coordinator
Posted 1 day ago
Job Viewed
Job Description
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Research Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve data entry, query resolution and admin.
Bonus to have:
Experience with Oncology
Clinical Research Physician
Posted 1 day ago
Job Viewed
Job Description
Planet Pharma are partnered with a leading clinical research organisation, who are seeking an experienced Research Physician with a strong clinical background and the ability to make independent decisions in a research environment.
Requirements:
- Minimum of 4 years’ experience in the NHS at Registrar level, including independent decision-making on the ward and running outpatient clinics.
- Background in General Medicine / Acute Internal Medicine.
- MRCP qualification.
- GMC registered – candidates must provide their GMC number.
- Right to work in the UK.
- Experience or exposure to clinical trials would be highly advantageous.
Candidates must be proactive, clinically competent, and ready to contribute to high-quality research delivery.
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
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 recognized 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.
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Clinical Research Physician
Posted today
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Job Description
We are seeking to appoint a CRP1 (Clinical Research Physician – level 1) to join our dedicated team at our clinic in Teesside. The focus of this role is to fulfil the role of Sub-Investigator and Principal Investigator (where delegated) in clinical research studies in compliance with the protocol and ICH/GCP.
We welcome applications from newly qualified doctors with 2 years of experience (FY 1&2 included) and no prior experience in clinical research. This is an ideal opportunity for candidates exploring an alternative to NHS or private sector.
If you have prior experience in research or you have a real interest in changing to a career in clinical research and bring additional years of experience, particularly in psychiatry, then we would like to hear from you too
Starting salary: £50,000
(additional considerations will be made for those that match some/all of the "desirable" criteria outlined in Key Skills)
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
Essential
- UK GMC Registered with valid licence to practice
- 2 years post graduate experience of working as a doctor in the UK within the NHS (minimum)
Desirable
- 2+ Years of UK clinical experience in any specialty
- 2+ years of psychiatry experience
- Previous clinical research experience in SMO/CRO
RESPONSIBILITIES:
Clinical activities:
- Fulfil the role of Sub Investigator / Principal Investigator where delegated.
- Provision of medical care and oversight of clinical trial participants.
- Ensure trial related procedures are completed in accordance with ICH-GCP guidelines and in compliance with the protocol.
- Review medical records of potential study participants.
- Remain proactive in participants study visits, including taking informed consent, physical examinations and other clinical procedures.
- Ensure that study documentation is completed, signed off, and actioned, as appropriate.
- Maintain accurate source notes.
- Review medical reports and lab results.
- Assist clinical staff members in various clinical activities as required.
- Participate in site monitoring visits with Clinical Research Associates.
- Ensure timelines for data queries are achieved.
- Continuously work towards maintaining and improving quality in all areas.
- On-call rota duties as required.
- Assess and review memory clinic patients (only applicable to sites where MAC operates a memory clinic)
Management:
- Attend Investigator Meetings (IM), Site Initiation Visits (SIV) and Pre-Study Selection Visits (PSSV) as required.
- Review source documents.
- Participate in sponsor and regulatory audits as required.
- Participate in meetings with colleagues and customers.
Leadership
- Provide practical help and guidance to other staff.
- Instil confidence in patients, customers and colleagues.
- Providing training to the clinical/ recruitment teams on essential medical information and protocols when required.
Commercial Awareness and Contribution to Targets
- Maintain an awareness of our key customers and market competitors.
- Share ideas from previous work environments to enhance current role.
- Maintain an awareness of site KPI's and contribute positively to meeting these targets.
Professional development
- Always maintain a professional attitude and appearance to customers/colleagues.
- Ensure that GMC requirements for revalidation are met appropriately to retain license to practice.
- Identify opportunities for self-development.
Recruitment:
- Assist with the development of recruitment strategy with the Envision team as a therapy area specialist.
- Maintain awareness of chat and screen fails and patient drop-out rates, taking appropriate corrective action.
- Keep up to date with study status, ensuring each stage is optimised.
- Establish and maintain relationships with local GPs, Consultants and service providers.
General:
- Share experience and knowledge with colleagues as appropriate and in an appropriate manner.
- Compliance with MAC policy on equality and diversity
- To maintain professional qualifications required for the role, including continuous personal development
- To work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clinical Practice
- To work according to MAC SOPs, guidelines and policies
- To work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business-related data.
- To maintain a high level of initiative and personal responsibility, liaising appropriately with team members and managers to ensure your job role is efficiently carried out
- To support the aims of MAC and to represent MAC appropriately in a professional way to all our customers
PHYSICAL, WORK ENVIRONMENT, TRAVEL DEMANDS:
- Dealing with bodily fluids.
- Long periods looking at a computer screen.
- Meeting deadlines and working within strict timelines.
- Ability to travel between sites if required.
- Ability to travel to national/international meetings.
BENEFITS:
- Health Insurance
- Eye Care Vouchers
- Cycle to work scheme
- Free onsite parking
- 25 days annual leave (increasing in increments to 30 days after 6 years' service)
- Your birthday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Please email should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.
Clinical Research Associate
Posted 14 days ago
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Job Description
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
With access to world-class training and professional development, we'll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
*Please note - this role is not eligible for UK visa sponsorship*
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 Manager
Posted 2 days ago
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Job Description
Key Responsibilities:
- Plan, initiate, and manage clinical research studies from protocol development to final report.
- Ensure compliance with all relevant regulatory guidelines (e.g., ICH-GCP, FDA, MHRA) and ethical principles.
- Recruit, train, and supervise clinical research staff, including coordinators and investigators.
- Develop and manage research budgets, ensuring efficient allocation of resources.
- Oversee participant recruitment and retention strategies.
- Manage data collection, monitoring, and reporting processes, ensuring data accuracy and integrity.
- Liaise with regulatory authorities, ethics committees, sponsors, and other stakeholders.
- Develop and implement study protocols, informed consent forms, and other essential research documents.
- Conduct site initiation visits, monitoring visits, and close-out visits.
- Identify and mitigate research-related risks and issues.
- Prepare and submit study progress reports, adverse event reports, and final study reports.
- Contribute to the development of research strategies and the identification of new research opportunities.
- Bachelor's degree in a life science, nursing, or related field; Master's degree preferred.
- Proven experience in clinical research management, with a strong understanding of GCP guidelines.
- Demonstrated success in managing multiple clinical trials simultaneously.
- Excellent knowledge of regulatory requirements and ethical considerations in research.
- Strong leadership, communication, and interpersonal skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to develop and manage budgets effectively.
- Strong analytical and problem-solving skills.
- Experience in (mention specific therapeutic area if applicable, e.g., oncology, cardiology) is a plus.
- Relevant certifications (e.g., ACRP, SOCRA) are desirable.