22 Iqvia jobs in Farnborough

Building on our track record of delivering pioneering research we are working in collaboration with Cambridge University Hospitals NHS Trust, University of Cambridge and the Cancer Research UK (CRUK) Queen Mary University of London Cancer Prevention Trials Unit (CPTU) to deliver a clinical trial into the early detection of Oesophageal Cancer, the BEST4 Screening Study.  

This is an exciting project funded by CRUK and the National Institute for Health Research (NIHR). The trial aims to determine whether the Capsule Sponge test can be used to determine early diagnosis of cancer of the oesophagus and reduce the number of deaths due to oesophageal cancer.   

The BEST4 screening study will recruit 120,000 participants, of whom will be invited for a Capsule Sponge test on the BEST4 mobile units located in approximately 5 regions across the UK. To support this study, we are recruiting Clinical Research Practitioners to work across different locations (within a designated region). This is an exciting opportunity to be involved in a ground-breaking clinical trial and work across different locations carrying out clinical trial activities to ensure the successful delivery and recruitment of the BEST4 study.    

You will be responsible for managing clinics on the BEST4 mobile unit and will be trained to administer the Capsule Sponge test. You will work alongside established clinical teams, researchers, research nurses, research practitioners and administrators to facilitate recruitment, sample collection, data entry and providing clinical support as required. You will therefore be required to travel to various sites and undertake clinics in a mobile unit.  

You will also need to liaise closely with the National Clinical Coordinator regarding appointments and cover on the unit. You will work closely with the National Clinical Coordinator, Clinical Research Team and Project managers at QMUL, Cambridge and EMS to ensure we meet the study objectives. You will be responsible for ensuring clinical and regulatory compliance, and that each participant journey and their individual experience is to the highest standard, which is a vital part of this role.  

Requirements

Main Duties 

We seek a motivated, enthusiastic and flexible candidate to join the BEST4 team. This is a clinical patient facing post, which requires a dynamic individual who can work both independently and as part of a team. 

A full programme of induction and ongoing support will be provided to the successful candidate. 

Main duties include: 

• Managing the clinic on the BEST4 mobile unit. 

• Promote and nurture a welcoming, professional and pleasant environment for all participants. 

• Be able to provide and receive complex information in the process of explaining study involvement and obtaining informed consent.   

• Complete the BEST4 participant screening visit as per study protocol.  

• To confirm the participant is safe and able to take part in the study. 

• Complete the informed consent process with the participant prior to the Capsule Sponge test.  

• To complete the Capsule Sponge test on the participant.   

• Work autonomously to manage their caseload of participants, whilst working as part of a wider BEST4 research team.  

• Perform other clinical skills, as required, to care for participants during their study visit (e.g. emergency practices). 

• Work in accordance with local policy and procedures and be able to take appropriate action in case of emergencies (detachment, bleeding, resuscitation or anaphylactic reaction) 

• Ensure that mandatory training is kept up to date as per local policies and requirements.  

• Work closely with the BEST4 clinical coordinator to address areas where re-training in Capsule Sponge test administration might be required. 

• Responsible for Inputting and data onto the electronic Case Report Form (eCRF) and other related research databases as required.  

• Collects, records, verifies and enters study data with a high degree of accuracy and in accordance with the principles of ICH Good Clinical Practice (ICH GCP). 

• Work in accordance with regulations as described in ICH-GCP, National Directives and Research Governance of Cambridge University, the Trusts, CPTU and EMS Healthcare policies and procedures. 

• To identify potential barriers to recruitment and be involved in implementing action/plans as required. 

• Facilitate and maintain effective communication with the study team, BEST4 Research Practitioners and study participants. To attend and contribute to meetings relevant to the BEST4 study and mobile units.  

• Liaise with various study personnel at Cambridge University Hospitals NHS Trust, University of Cambridge, CPTU and EMS Healthcare as necessary. 

• Responsible for driving the BEST4 mobile units to the different research sites as per the study schedule. 

Qualifications

• Relevant healthcare qualification (e.g. Paramedic, Midwife, Radiographer, Dietitian or equivalent)
• Continued CPD

Experience

• Clinical experience working with patients
• Significant clinical experience working with patients
• Experience in working as part of a multidisciplinary healthcare team
• A good understanding of clinical research

Skills

• Excellent interpersonal and communication skills (verbal/written)
• Ability to work accurately and methodically with excellent attention to detail
• A team player, whilst possessing ability to work independently and on their own initiative
• High level of organisational and time management skills
• Excellent IT knowledge/skills and proficient in MS Office Software

Other

• Full, Clean UK Manual Driving Licence. Travel to various sites, and drive the clinical mobile unit (requiring only a standard car driving licence) to support delivery of study activities.
• Willing to travel and complete overnight stays as required

Qualifications

• Degree in a related subject area
• Registered Nurse (NMC)
• ICH GCP Training
• Training on Basic Life Support (BLS) or Immediate Life Support

Experience

• Prior research experience
• Upper GI or endoscopy experience
• Experience in Cancer Research
• Experience in Nurse led/Practitioner led clinics
• Prior experience of working with Capsule Sponge device

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 Practitioner - click apply now!

Building on our track record of delivering pioneering research we are working in collaboration with Cambridge University Hospitals NHS Trust, University of Cambridge and the Cancer Research UK (CRUK) Queen Mary University of London Cancer Prevention Trials Unit (CPTU) to deliver a clinical trial into the early detection of Oesophageal Cancer, the BEST4 Screening Study.  

This is an exciting project funded by CRUK and the National Institute for Health Research (NIHR). The trial aims to determine whether the Capsule Sponge test can be used to determine early diagnosis of cancer of the oesophagus and reduce the number of deaths due to oesophageal cancer.   

The BEST4 screening study will recruit 120,000 participants, of  whom will be invited to receive the Capsule Sponge test on the BEST4 mobile units located in approximately 5 regions across the UK. To support this study, we are recruiting Clinical Research Nurses to work across different locations (within a designated region). This is an exciting opportunity to be involved in a ground-breaking clinical trial and work across different locations carrying out clinical trial activities to ensure the successful delivery and recruitment of the BEST4 study.   

You will be responsible for managing clinics on the BEST4 mobile unit and will be trained to administer the Capsule Sponge test. You will work alongside established clinical teams, researchers, research nurses and administrators to facilitate recruitment, sample collection, data entry and providing clinical support as required. You will therefore be required to travel to various sites and undertake clinics in a mobile unit.  

You will also need to liaise closely with the clinic coordinator regarding appointments and cover on the unit. You will work closely with the Clinical Coordinator, Clinical Research Team and Project managers at QMUL, Cambridge and EMS to ensure we meet the study objectives. You will be responsible for ensuring clinical and regulatory compliance, and that each participant journey and their individual experience is to the highest standard, which is a vital part of this role.  

Requirements

We seek a motivated, enthusiastic and flexible candidate to join the BEST4 team. This is a clinical patient facing post, which requires a dynamic individual who can work both independently and as part of a team. 

A full programme of induction and ongoing support will be provided to the successful candidate. 

Main duties include: 

• Managing the clinic on the BEST4 mobile unit
• Promote and nurture a welcoming, professional and pleasant environment for all participants. 
• Be able to provide and receive complex information in the process of explaining study involvement and obtaining informed consent.   
• Complete the BEST4 participant screening visit as per study protocol.  
• To confirm the participant is safe and able to take part in the study. Complete the informed consent process with the participant prior to the Capsule Sponge test.  
• To complete the Capsule Sponge test on the participant.   
• Work autonomously to manage their caseload of participants, whilst working as part of a wider BEST4 research team.  
• Perform other clinical skills, as required, to care for participants during their study visit (e.g. emergency practices). 
• Work in accordance with local policy and procedures and be able to take appropriate action in case of emergencies (detachment, bleeding, resuscitation or anaphylactic reaction) 
• Ensure that mandatory training is kept up to date as per local policies and requirements.  
• Work closely with the BEST4 clinical coordinator to address areas where re-training in Capsule Sponge test administration might be required. 
• Responsible for Inputting and  data onto the electronic Case Report Form (eCRF) and other related research databases as required.  
• Collects, records, verifies and enters study data with a high degree of accuracy and in accordance with the principles of ICH Good Clinical Practice (ICH GCP). 
• Work in accordance with regulations as described in ICH-GCP, National Directives and Research Governance of Cambridge University, the Trusts, CPTU and EMS Healthcare policies and procedures. 
• To identify potential barriers to recruitment and be involved in implementing action/plans as required. 
• Facilitate and maintain effective communication with the study team, BEST4 Research Nurses and study participants. To attend and contribute to meetings relevant to the BEST4 study and mobile units.  
• Liaise with various study personnel at Cambridge University Hospitals NHS Trust, University of Cambridge, CPTU and EMS Healthcare as necessary. 
• Responsible for driving the BEST4 mobile units to the different research sites as per the study schedule. 

Criteria - Essential:

• Registered nurse (NMC Registration) 
• Continued CPD 
• Previous research experience or Upper GI experience 
• Significant post-registration clinical experience 
•  Experience in performing nurse-led clinics.
• A good understanding of clinical research  
• Excellent interpersonal and communication skills (verbal/written)  
• Ability to work accurately and methodically with excellent attention to detail. 
• A team player, whilst possessing ability to work independently and on their own initiative. 
• High level of organisational and time management skills. 
• Excellent IT knowledge / skills and proficient in MS Office Software. 
• Full, Clean UK Driving Licence
• Willing to travel and complete overnight stays as required.
• Motivated and enthusiastic 

Criteria - Desirable

• Degree in a related subject area 
• ICH GCP Training 
• Knowledge of research regulations at national level. 
• Prior experience in cancer research and endoscopy.  
• Prior experience of working with Capsule Sponge device.  

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 Nurse - click apply now!

• Perform remote monitoring of clinical trial sites to ensure compliance with protocols, regulatory requirements, and GCP.
• Verify the accuracy, completeness, and integrity of clinical data through source data verification and query resolution.
• Ensure the safety and rights of study participants are protected at all times.
• Conduct remote site initiation, monitoring, and close-out visits.
• Review and maintain essential study documents, including investigator site files and regulatory binders.
• Provide training and ongoing support to site staff regarding trial protocols and procedures.
• Identify, document, and escalate any deviations from protocol or GCP.
• Manage communication between study sites, the sponsor, and other relevant stakeholders.
• Prepare and submit monitoring reports in a timely manner.
• Contribute to the development and review of study-related documents as needed.

• Bachelor's degree in a life science, nursing, pharmacy, or a related scientific discipline.
• Minimum of 3-5 years of direct experience as a Clinical Research Associate.
• Thorough understanding of ICH-GCP guidelines and other relevant regulatory requirements.
• Proven experience in clinical trial monitoring, ideally with remote monitoring capabilities.
• Excellent understanding of clinical trial processes from start-up to close-out.
• Strong data management and analytical skills.
• Exceptional written and verbal communication skills.
• Demonstrated ability to work independently, manage time effectively, and meet strict deadlines.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel for occasional site visits if required, though the role is primarily remote.

• Conduct pre-study, initiation, interim, and close-out visits for clinical trial sites according to approved protocols and company SOPs.
• Ensure timely recruitment of subjects and adherence to inclusion/exclusion criteria.
• Verify the accuracy, completeness, and integrity of clinical data through source data verification (SDV).
• Monitor subject safety and report adverse events (AEs) and serious adverse events (SAEs) according to regulatory requirements.
• Train and mentor site staff on study-specific procedures, protocols, and regulatory compliance.
• Build and maintain strong working relationships with investigators, site staff, and study sponsors.
• Ensure compliance with all applicable regulatory requirements, including ICH-GCP guidelines.
• Manage site budgets and timelines effectively.
• Prepare and submit site monitoring reports in a timely and accurate manner.
• Participate in the selection and qualification of new clinical investigators and sites.
• Address site-related issues and implement corrective actions as needed.
• Contribute to the development and review of study protocols and other essential trial documents.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is advantageous.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or equivalent role.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials in the UK and EU.
• Proven experience in monitoring multiple clinical trial sites.
• Excellent understanding of medical terminology and clinical trial processes.
• Strong site management and communication skills.
• Ability to travel extensively to study sites (estimated 50-60% travel).
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Excellent organizational, analytical, and problem-solving skills.
• Ability to work independently and as part of a cross-functional team.
• Strong written and verbal communication skills.

• Conducting site visits, including pre-study, initiation, routine monitoring, and close-out visits.
• Ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP).
• Verifying the accuracy, completeness, and integrity of clinical data through source data verification.
• Monitoring patient safety and reporting adverse events.
• Managing study-related documentation and regulatory binders.
• Liaising with investigators and site staff to resolve queries and ensure protocol compliance.
• Training and mentoring site personnel on study procedures.
• Contributing to the development of study protocols and other trial-related documents.
• Maintaining effective communication with internal project teams and external stakeholders.
• Ensuring timely completion of trial milestones.

• Bachelor's degree in life sciences, nursing, pharmacy, or a related field; advanced degree preferred.
• Proven experience as a Clinical Research Associate (CRA) with a strong understanding of clinical trial operations.
• In-depth knowledge of GCP guidelines and regulatory requirements.
• Excellent monitoring skills and experience with source data verification.
• Proficiency in CTMS and EDC systems.
• Strong analytical and problem-solving abilities.
• Exceptional communication, interpersonal, and presentation skills.
• Ability to travel to clinical sites, with a valid driving licence.
• Detail-oriented and highly organised.
• Ability to work independently and manage multiple priorities effectively in a hybrid work model.