385 Trial Management jobs in the United Kingdom
Senior Clinical Trial Administrator
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Clinical Trial Manager
Posted today
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Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.
You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.
We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.
About You
- You love having responsibility and a say in how clinical trials are run
- You plan ahead, but have alternative options and a flexible approach
- You are client focused
- You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
- You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly
- You are a master at identifying any risks that threaten projects and handle them resolutely
- You thrive and work with autonomy and ownership to deliver successful outcomes
- Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
- Successful execution of assigned trials and ensuring completion of trial deliverables
- Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
- Mentoring and training of team members
- Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
- Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
- Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction
Minimum Required:
- Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology
- Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).
- Significant clinical trial management experience in the area of oncology
- Working knowledge of GCP/ICH guidelines and the clinical development process
- Availability for domestic and international travel including overnight stays
- Must be able to communicate effectively in the English language
- Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
- Demonstrated ability to develop positive working relationships with internal and external organizations
- Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
- Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
Clinical Trial Manager
Posted today
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Clinical Trial Manager
Location: London, UK (Hybrid – 3 to 4 days/week)
Job Type: Part-time (flexible)
Industry: Clinical
Therapeutic Areas: Oncology, Respiratory
Job Purpose:
As a Clinical Trial Manager (CTM), you will oversee the planning, execution, and close-out of clinical trials to ensure they are conducted to the highest standards of quality, compliance, and patient safety.
Key Responsibilities:
- Lead and manage the execution of assigned clinical trials from start-up through to completion.
- Coordinate cross-functional project teams including CRAs, data managers, regulatory, and medical affairs.
- Develop and monitor timelines, budgets, and risk mitigation plans.
- Serve as the primary point of contact for sponsors, sites, and vendors.
- Monitor site performance and recruitment, proactively resolving site issues.
- Ensure compliance with ICH-GCP, SOPs, and all regulatory guidelines.
- Contribute to protocol development and support study documentation review.
Performance Expectations:
- Deliver clinical trials on time, within budget, and to the expected quality and regulatory standards.
- Maintain excellent CRO/site/vendor relationships and ensure effective trial oversight.
- Ensure complete, accurate, and timely documentation and data collection.
- monitor patient recruitment, resolving challenges swiftly.
- Ensure data quality and integrity, ensuring alignment with study protocols.
- Communicate effectively across project stakeholders and lead team meetings.
- Manage trial risks effectively
- Demonstrate full compliance with GCP and all internal/external standards.
Requirements:
- Minimum 5 years of clinical trial management experience in a CRO or pharmaceutical setting.
- Proven expertise in oncology and respiratory trials.
- Strong knowledge of Good Clinical Practice (GCP) and global regulatory requirements.
- Hands-on experience with Electronic Data Capture (EDC) systems and CTMS platforms.
- Exceptional organizational, communication, and leadership skills.
- Ability to work independently and collaboratively in a cross-functional team.
Compensation & Benefits:
- Salary: £55,000 – £70,000 per annum (pro-rated for part-time), based on experience.
- Bonus: Annual performance-related bonus.
- Pension Scheme: Employer-matched contributions.
- Private Medical Insurance, mental health resources, and wellness support.
- Life Assurance and income protection.
- 25 days annual leave plus bank holidays (pro-rated for part-time).
- Flexible hybrid working, with 3–4 days/week in the London office.
- professional development
Clinical Trial Manager
Posted today
Job Viewed
Job Description
Clinical Trial Manager
Location: London, UK (Hybrid – 3 to 4 days/week)
Job Type: Part-time (flexible)
Industry: Clinical
Therapeutic Areas: Oncology, Respiratory
Job Purpose:
As a Clinical Trial Manager (CTM), you will oversee the planning, execution, and close-out of clinical trials to ensure they are conducted to the highest standards of quality, compliance, and patient safety.
Key Responsibilities:
- Lead and manage the execution of assigned clinical trials from start-up through to completion.
- Coordinate cross-functional project teams including CRAs, data managers, regulatory, and medical affairs.
- Develop and monitor timelines, budgets, and risk mitigation plans.
- Serve as the primary point of contact for sponsors, sites, and vendors.
- Monitor site performance and recruitment, proactively resolving site issues.
- Ensure compliance with ICH-GCP, SOPs, and all regulatory guidelines.
- Contribute to protocol development and support study documentation review.
Performance Expectations:
- Deliver clinical trials on time, within budget, and to the expected quality and regulatory standards.
- Maintain excellent CRO/site/vendor relationships and ensure effective trial oversight.
- Ensure complete, accurate, and timely documentation and data collection.
- monitor patient recruitment, resolving challenges swiftly.
- Ensure data quality and integrity, ensuring alignment with study protocols.
- Communicate effectively across project stakeholders and lead team meetings.
- Manage trial risks effectively
- Demonstrate full compliance with GCP and all internal/external standards.
Requirements:
- Minimum 5 years of clinical trial management experience in a CRO or pharmaceutical setting.
- Proven expertise in oncology and respiratory trials.
- Strong knowledge of Good Clinical Practice (GCP) and global regulatory requirements.
- Hands-on experience with Electronic Data Capture (EDC) systems and CTMS platforms.
- Exceptional organizational, communication, and leadership skills.
- Ability to work independently and collaboratively in a cross-functional team.
Compensation & Benefits:
- Salary: £55,000 – £70,000 per annum (pro-rated for part-time), based on experience.
- Bonus: Annual performance-related bonus.
- Pension Scheme: Employer-matched contributions.
- Private Medical Insurance, mental health resources, and wellness support.
- Life Assurance and income protection.
- 25 days annual leave plus bank holidays (pro-rated for part-time).
- Flexible hybrid working, with 3–4 days/week in the London office.
- professional development
Clinical Trial Manager
Posted today
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Job Description
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.
About this role
We're looking for a Clinical Trial Manager with experience in opthalmology clinical trials to join our FSP team , supporting a biotechnology company. You'll lead complex studies and help advance treatments that make a real difference for patients.
Responsibilities
- Oversee trial execution (start-up to closeout)
- Manage CROs, vendors, and site relationships
- Support protocol and consent development
- Ensure regulatory compliance (ICH-GCP, FDA, etc.)
- Track budgets, timelines, and quality metrics
- Help prepare for audits and submissions
Requirements
- 1–3 years in clinical trial/project management (biotech, CRO, or pharma)
- Degree in life sciences or related field
- Strong communication, problem-solving, and organizational skills
- Familiarity with global trial regulations and study phases
- Bonus: Ophthalmology experience
What We Offer
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients
A Bit More About Us
Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.
Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.
#Together we make a difference
Clinical Trial Manager
Posted today
Job Viewed
Job Description
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.
About this role
We're looking for a Clinical Trial Manager with experience in opthalmology clinical trials to join our FSP team , supporting a biotechnology company. You'll lead complex studies and help advance treatments that make a real difference for patients.
Responsibilities
- Oversee trial execution (start-up to closeout)
- Manage CROs, vendors, and site relationships
- Support protocol and consent development
- Ensure regulatory compliance (ICH-GCP, FDA, etc.)
- Track budgets, timelines, and quality metrics
- Help prepare for audits and submissions
Requirements
- 1–3 years in clinical trial/project management (biotech, CRO, or pharma)
- Degree in life sciences or related field
- Strong communication, problem-solving, and organizational skills
- Familiarity with global trial regulations and study phases
- Bonus: Ophthalmology experience
What We Offer
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients
A Bit More About Us
Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.
Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.
#Together we make a difference
Clinical Trial Manager
Posted today
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Job Description
Clinical Trial Manager – Virology | London (3-5 Days Onsite)
Join a leading sponsor client driving cutting-edge Phase Ib-III virology clinical trials across the EMEA region on a 12 month contracted role . As Clinical Trial Manager, you will play a pivotal role in managing regional components of global studies, ensuring timely delivery and quality execution in partnership with CROs and cross-functional teams.
Key Responsibilities:
- Regional management of Phase Ib-III clinical trials for a sponsor client
- Coordination of study documents including protocols, informed consents, monitoring plans
- Manage CROs/vendors and train study teams on protocol adherence
- Support study monitoring/co-monitoring and regulatory compliance
- Collaborate closely with global and local stakeholders to ensure study progress
- Assist in study budgeting, SOP implementation, and troubleshooting
What We’re Looking For:
- Proven clinical trial management experience at senior CTMA level
- Relevant scientific background (BSc or nursing qualification)
- Familiarity with FDA, EU regulations, ICH guidelines, and GCP
- Experience with virology studies advantageous but not essential
- Strong organizational, communication, and teamwork skills
- Ability to multitask and adapt in a fast-paced environment
- Willingness for occasional international travel
Why Join?
- Work for a prestigious sponsor client with a global impact
- Lead and influence multiple virology clinical studies
- Competitive package and career growth opportunities
- Located in central London with flexible onsite attendance (3-5 days/week)
Interested? Contact us today for a confidential discussion or apply now!
Clinical Trial Manager
Posted today
Job Viewed
Job Description
Clinical Trial Manager – Virology | London (3-5 Days Onsite)
Join a leading sponsor client driving cutting-edge Phase Ib-III virology clinical trials across the EMEA region on a 12 month contracted role . As Clinical Trial Manager, you will play a pivotal role in managing regional components of global studies, ensuring timely delivery and quality execution in partnership with CROs and cross-functional teams.
Key Responsibilities:
- Regional management of Phase Ib-III clinical trials for a sponsor client
- Coordination of study documents including protocols, informed consents, monitoring plans
- Manage CROs/vendors and train study teams on protocol adherence
- Support study monitoring/co-monitoring and regulatory compliance
- Collaborate closely with global and local stakeholders to ensure study progress
- Assist in study budgeting, SOP implementation, and troubleshooting
What We’re Looking For:
- Proven clinical trial management experience at senior CTMA level
- Relevant scientific background (BSc or nursing qualification)
- Familiarity with FDA, EU regulations, ICH guidelines, and GCP
- Experience with virology studies advantageous but not essential
- Strong organizational, communication, and teamwork skills
- Ability to multitask and adapt in a fast-paced environment
- Willingness for occasional international travel
Why Join?
- Work for a prestigious sponsor client with a global impact
- Lead and influence multiple virology clinical studies
- Competitive package and career growth opportunities
- Located in central London with flexible onsite attendance (3-5 days/week)
Interested? Contact us today for a confidential discussion or apply now!
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Clinical Trial Manager - Virology
Posted today
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Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.
Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis. In this role, you will oversee regional management of clinical trials (Phase Ib-III) with a focus on the EMEA region. You will work closely with global teams and external partners to ensure the successful execution of studies from start-up to close-out. This position requires a mix of onsite presence (3-5 days per week) and remote work.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Manage regional aspects of clinical trials, ensuring timelines and budgets are met.
- Draft and review key study documents such as protocols, consent forms, and reports.
- Collaborate with vendors and CROs to execute studies effectively.
- Monitor study progress and address any issues that arise.
- Train investigators, coordinators, and vendors on study requirements.
- Oversee site budget and contract processes.
- Support data review and preparation of study reports.
- Contribute to study logistics, planning, and stakeholder management.
- Provide expertise on country-specific regulations and site suitability.
- Participate in cross-functional team activities and initiatives.
Key Skills and Requirements:
- Background in a scientific discipline or nursing qualification.
- Experience in managing or coordinating clinical studies.
- Familiarity with virology is beneficial but not essential.
- Knowledge of FDA, EU regulations, ICH guidelines, and GCP standards.
- Strong organizational, communication, and problem-solving skills.
- Ability to prioritize tasks and adapt to changing environments.
- Monitoring or co-monitoring experience is desirable.
- Willingness to travel internationally as needed.
For more information, please contact Athi Singata .
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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Clinical Research Coordinator
Posted 16 days ago
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Job Description
Job Title: Clinical Research Coordinator (Band 6 Nurse)
Contract Type: Part-Time (2–3 days/week)
Overview:
We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.
Key Responsibilities:
- Identify and recruit eligible patients for clinical trials.
- Perform accurate and timely data entry into study databases.
- Collaborate with research and clinical teams to ensure protocol compliance.
- Maintain high standards of documentation and regulatory adherence.
Requirements:
- Registered Band 6 Nurse with relevant clinical experience.
- Demonstrated experience in patient identification and data entry.
- Strong attention to detail and organizational skills.
- Must be available to work every Wednesday, plus two additional weekdays.
Please submit your CV or get in touch via email:
Clinical Research Coordinator
Posted 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