63 Clinical Trials jobs in the United Kingdom

Job Title: Clinical Trials Manager

Location: London

Contract: 5 months

Hours: 14.5 hours per week (9-5 Mondays/Tuesday)

Rates: 22.79-23.97 p/h

Job Description

SRG are looking for a clinical trials manager to join a leading higher educations provider based in London. The primary role of the post holder is to set up and support a high quality clinical trial at the CCTU.

Duties and Responsibilities

• To establish and maintain effective management systems for the trial
• To act as the central Trials Unit contact for the Trial
• To work closely with the Chief Investigator, trial and IT staff to ensure the successful management of the Trial.
• Secure all necessary approvals for the trial and participating sites according to the UK regulations including UK Research Governance Framework
• Coordinate the design, printing and distribution of trial documentation
• Develop trial specific documentation that is compliant with the CCTU Policies and Standard Operating Procedures (SOPs) and ensure this is implemented and kept up to date.
• Ensure sites have appropriate training and maintain necessary records.
• Work within budget constraints in liaison with the Project Manager.
• Ensure that good communication is maintained between the CCTU and recruiting centre staff
• Provide updates on the progress of the trial at regular Trial Management Group meetings, to the Independent Data Monitoring and Trial Steering Committees and to the funder as required.
• Monitor the trial sites to assess compliance with the protocol and regulatory requirements.
• Prepare under the guidance of the Clinical Project Manager, the trial specifications for the Database.
• Undertake Risk Assessment of the trial and, with the Clinical Project Manager, propose appropriate mitigations.
• Minute trial related meetings.
• Supervise the data collected and enter data if required.
• Supervise the data cleaning and validation, including querying and chasing missing data in a timely manner.
• Monitor trial recruitment, providing support and motivation to recruiting staff as required.
• Ensure the timely submission and processing of data and documents from sites to the CTU including safety events. Prepare and submit the necessary reports to appropriate regulatory, ethical and other parties (such as submission of safety reports to the Ethics Committee).
• Represent the trial at conferences, meetings and internal unit meetings as appropriate.
• Keep the relevant literature searches up to date.
• Participate in university and the CCTU training and development initiatives.
• Carry out any other comparable tasks as required including being prepared to assist those working on other studies/trials as directed by the Head of Clinical Trial Operations.

Experience and Qualifications

• Degree and/or equivalent experience in Clinical Trials
• Experience of managing a clinical trial
• Experience of managing a trial of an investigational medicinal product
• Comprehensive understanding of UK Clinical Trials Regulations, ICH Good Clinical Practice, the European Directives on Clinical Trials and Good Clinical Practice and the Department of Health's Research Governance Framework
• Experience of monitoring
• Experience of using Pharmacovigilance systems
• Experience of working in an academic or similar institution
• Experience of public speaking and giving presentations
• Experience of data management
• Evidence of ability to set up and maintain effective management system in trials
• Excellent IT skills; MS Office Suite, Trial Databases and other Trial related systems (such as IMP management, Randomisation)
• Excellent communication and interpersonal skills
• A methodical and accurate approach to work with attention to detail
• The ability to make and carry out decisions and know when to confer with colleagues or refer matters onwards
• The ability to work without direct supervision; to manage own workload and display good organisational ability
• Take responsibility for setting and meeting targets for your own work and others
• Ability to evaluate risks inherent in clinical trials and decide those which should be prioritised to ensure that risks are properly managed
• Advanced organisational skills, managing several projects that are often time pressured, concurrently
• Ability to supervise other members of the team, promote good working relationships and resolve difficult situations
• Commitment to and knowledge of advancing equality, diversity and inclusion

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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A leading biotech company, with a well-established presence in multiple therapy areas is looking to hire a Lead Statistical Genetics Scientist to support the further development of their products.They have a track record of innovation and a highly collaborative, cross-functional work environment.You would be joining an established team with significant expertise within genetics an.

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Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time role is to support a site in Halifax, West Yorkshire in conducting a clinical trial for 15 hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Plan and coordinate logistical activity for study procedures according to the study protocol
• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correct custody of study drug according to site standard operating procedures
• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
• Good organizational skills with the ability to pay close attention to detail.

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time role is to support a site in Oldham in conducting a clinical trial for 16 hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Plan and coordinate logistical activity for study procedures according to the study protocol
• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correct custody of study drug according to site standard operating procedures
• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
• Good organizational skills with the ability to pay close attention to detail.

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:

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.

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.