863 Clinical jobs in the United Kingdom

The Clinical Research Study Coordinator will play a key role in supporting the delivery of high-quality clinical trials focused on obesity and metabolic health across Greater Manchester. Based within EMS’ mobile and fixed-site research infrastructure, you will be responsible for coordinating study operations, participant engagement, and ensuring smooth study delivery in line with protocols and regulatory requirements. 
 
This role offers an exciting opportunity to work on a high-profile obesity study while contributing to a broader range of EMS clinical research activities. The ideal candidate will have prior experience coordinating clinical research studies and be confident working independently in a fast-paced, participant-focused setting. 

Location: Greater Manchester

1 year fixed contract 

Monday-Friday 37.5 hour week

Salary range: £30K-£36K depending on experience

Requirements

Main Duties 

• Coordinate day-to-day operational aspects of assigned clinical studies, ensuring alignment with protocols, GCP, and EMS SOPs. 

• Schedule and manage participant visits, including screening, enrolment, and follow-up activities. 

• Maintain detailed, accurate study documentation, including source data, CRFs, logs, and regulatory binders. 

• Collaborate with clinical staff, including nurses and investigators, to ensure study timelines and objectives are met. 

• Support participant retention and compliance through effective communication and follow-up. 

• Assist in the setup and maintenance of study equipment, supplies, and site readiness. 

• Liaise with the data management team to ensure timely entry, verification, and query resolution. 

• Participate in site meetings, staff training, monitoring visits, and audits as required. 

• Ensure participant safety, confidentiality, and adherence to ethical and regulatory standards. 

• Contribute to continuous improvement and operational excellence across the EMS Study portfolio. 

Experience - Essential  

• Experience coordinating or supporting clinical research studies in an NHS, academic, or commercial setting. 

• Understanding of ICH-GCP and regulatory frameworks governing clinical trials. 

• Demonstrated ability to manage participant interactions and study workflows. 

• Strong organisational skills with the ability to manage competing priorities. 

•  Confident using electronic data capture systems or clinical databases. 

Experience - Preferable 

• Experience working in obesity, metabolic health, or lifestyle-related trials. 

•  Familiarity with community-based or mobile clinical research delivery models. 

• Prior experience working with underserved or diverse populations. 

Key Skills  

• Excellent written and verbal communication. 

• Detail-oriented with a focus on data integrity and participant safety. 

• Flexible and proactive team player. 

• Strong time management and problem-solving skills. 

• Technologically proficient, especially with study software and electronic documentation tools. 

Other Requirement  

• Full UK residency and right to work. 

• Valid UK driving licence and willingness to travel across Greater Manchester and EMS sites as needed. 

• Flexibility to work early mornings, evenings, or weekends depending on study needs. 

Benefits

You work hard for us; we work hard for you. It is that simple. And we know, it sounds too good to be true (we hear that a lot). But trust us, this could be the best decision you make. 

• Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years 

• 1 Occasion Day each year; this could be your child’s first day of school, their nativity play, or your own birthday – the choice is yours! 

• Healthshield 

• Subsidised company events and gatherings  

• A gift for your birthday  

• Well being support from our qualified Mental Health First Aiders, as well as via our health scheme 

If you want to join us as our Clinical Research Study Coordinator - click apply now!

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.

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.

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.

A global pharmaceutical company is currently looking for a Senior Clinical Data Manager to join their team on an 9 to 12-month temporary contract.

As a senior leader in the team, you'll play a critical part in designing streamlined, risk-based data strategies that drive quality and efficiency from protocol to archive. You'll collaborate across functions and help shape the future of trial delivery.

Key Responsibilities

• Lead the creation of an agile, tech-driven data management operating model aligned with best practices.
• Evaluate and implement emerging technologies (EDC, integration platforms, analytics tools) to modernise data workflows
• Embed regulatory standards and quality-by-design principles across all data management activities
• Act as a strategic partner across clinical operations, stats, programming and monitoring, ensuring a cohesive, risk-based trial delivery approach

Requirements

• Strong experience in clinical data management with deep operational and technical expertise
• Proven success leading complex process and technology transformations
• Strong grasp of risk-based approaches, centralised monitoring and data quality frameworks
• Excellent communication and project leadership skills across cross-functional global teams

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 Business in relation to this role.

A global pharmaceutical company is currently looking for a Senior Clinical Data Manager to join their team on an 9 to 12-month temporary contract.

As a senior leader in the team, you'll play a critical part in designing streamlined, risk-based data strategies that drive quality and efficiency from protocol to archive. You'll collaborate across functions and help shape the future of trial delivery.

Key Responsibilities

• Lead the creation of an agile, tech-driven data management operating model aligned with best practices.
• Evaluate and implement emerging technologies (EDC, integration platforms, analytics tools) to modernise data workflows
• Embed regulatory standards and quality-by-design principles across all data management activities
• Act as a strategic partner across clinical operations, stats, programming and monitoring, ensuring a cohesive, risk-based trial delivery approach

Requirements

• Strong experience in clinical data management with deep operational and technical expertise
• Proven success leading complex process and technology transformations
• Strong grasp of risk-based approaches, centralised monitoring and data quality frameworks
• Excellent communication and project leadership skills across cross-functional global teams

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 Business in relation to this role.