Overview In this role you will monitor clinical studies across investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and applicable regulations. You will coordinate study setup and monitoring activities, including investigator...Read More>>.

Overview In this role you drive quality-driven clinical monitoring for investigator sites, ensuring studies run per protocol and regulatory standards. You work closely with sponsors and cross-functional teams, coordinating start-up, initiat...Read More>>.

Overview In this role you will support the advancement of clinical development by conducting on-site monitoring and oversight of trial activities. You’ll collaborate with sites to ensure protocol adherence, data integrity, and regulatory...Read More>>.

Overview As a CRA at Parexel, you will go beyond traditional monitoring to safeguard patient wellbeing and ensure study success across UK sites. You’ll manage site relationships, oversee quality from site identification to close-out, and...Read More>>.

Overview In this evergreen role, you contribute to a closely aligned sponsor partnership within a collaborative, quality-driven environment. You will monitor and support clinical studies at investigative sites, ensuring compliance with prot...Read More>>.

Overview In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data. You collaborate with sites to optimize subject recruitment and manage study documentation. You’ll track regu...Read More>>.

Overview You will support and oversee clinical studies from a home-based role in the UK or Northern Ireland, ensuring studies are conducted to protocol, SOPs, and ICH-GCP standards. You will coordinate study setup and monitoring activities,...Read More>>.

Overview As a Clinical Research Associate in Abbott Diabetes Care, you contribute to advancing diabetes care through clinical studies supporting innovative medical technologies. You’ll join a collaborative Clinical Affairs team in Witney,...Read More>>.

Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, wit...Read More>>.

Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sites and ensure that the study is conducted in compliance with the study protocol, ICH GCP and local regulatory requi...Read More>>.

Clinical Research AssociateLocation: Belfast / requires travel when requiredJob Purpose:Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sit...Read More>>.

Parexel FSP is hiring for an experienced Senior CRA level to join one of our large Sponsor’s in the EU. Some specifics about this advertised role This role is responsible for the site management, site monitoring and close-out o...Read More>>.

Senior Clinical Research Associate / Clinical Study ManagerSouthampton, Hampshire, United Kingdom (Sur site)Job DescriptionJob title: Senior Clinical Research Associate / Clinical Study ManagerDepartment:...Read More>>.

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable...Read More>>.

AbbVie seeks a field-based Clinical Research Associate (CRA) to advance AbbVie's pipeline by partnering with study teams, internal R&D stakeholders, investigators and site staff. You will ensure trial conduct, data integrity and patient safety whi...Read More>>.

Syneos Health is seeking a Senior CRA with UK monitoring experience to perform site qualification, initiation, monitoring, and close-out visits in a fast-paced, globally integrated environment. The role involves on-site and remote activities, ensu...Read More>>.

Single Sponsor Senior Clinical Research Associate (UK monitoring experience needed) Updated: Today Location: Remote, LND, United Kingdom Description Single Sponsor Senior Clinical Research Associate (U...Read More>>.

At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to s...Read More>>.

Research Associate in Mineral Construction Materials (SB13933) - Bath, BA2 7AYAbout the roleThe role is part of an exciting partnership with the University of Malaga in Spain, University of Manchester in the UK, and the European...Read More>>.

Research Associate (SB13960) - Bath, BA2 7AYAbout the roleAdvance Your Engineering Career Through Innovation and ImpactThe...Read More>>.

Research Associate/Fellow in Engineered Silk Manufacturing and Optical Fibre Technologies (SS13969) - Bath, BA2 7AYAbout the roleJoin the HOLLOW SILK project, an ambitious research project funded b...Read More>>.

Research Associate (SS13981) - Bath, BA2 7AYAbout the roleThe role is associated with the Royal Society International Collaboration Award “Operator learning for gradient flows with applications in imaging” led b...Read More>>.

Postdoctoral Research Associate (SS13987) - Bath, BA2 7AYThe Department of Mathematical Sciences at the University of Bath welcomes applications for an EPSRC-funded Research Associate in Analysis to work with Dr Matthew Schrecker in nonl...Read More>>.

Research associate in number theory (SS13993) - Bath, BA2 7AYAbout the roleApplications are invited for a postdoctoral research associate to work with Prof. Daniel Loughran as part of the EPSRC-funded programme gran...Read More>>.

Junior User Researcher - Associate Consultant - Digital Excellence - LondonReference Code: 350231-en_GBContract Type:PermanentProfessional Communities: Strategy & Transformation....Read More>>.

Postdoctoral Research Associate -Sutherland Building, Newcastle upon Tyne, Tyne and Wear, NE1 8ST, GBSalary: 41,064 - 46,049Work hours: Office Hours Monday to Friday, Full Time...Read More>>.

MSD is seeking a motivated Clinical Research Associate (CRA) to join our clinical operations team. The CRA serves as the primary site contact and site manager throughout all study phases, ensuring high-quality trial execution and compliance with I...Read More>>.

Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Oncology and Ophthalm...Read More>>.

IQVIA UK invites applications for Clinical Research Associates (CRAs) to join our Site Management team in Manchester. You will conduct site monitoring visits, support recruitment plans, ensure GCP/ICH compliance, and maintain TMF documentation....Read More>>.

AbbVie seeks a field-based Clinical Research Associate to support site monitoring and ensure trial integrity in the UK. You will partner with investigators and site staff to maintain high-quality conduct and patient safety throughout the study lif...Read More>>.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therap...Read More>>.

Syneos Health is seeking a Senior Clinical Research Associate with UK monitoring experience to oversee site qualification, initiation, monitoring and close-out visits, ensuring GCP compliance and patient safety across trials. The role requires up...Read More>>.

IQVIA is seeking an experienced Senior Clinical Research Associate to monitor and manage sites in the UK, ensuring protocol compliance and data quality. You will perform site visits, train sites, and collaborate with study teams to keep projects o...Read More>>.

The Cambridge-GSK Translational Immunology Collaboration (CG-TIC) invites applications for a Research Associate (Honorary Resident Doctor) based in the Department of Medicine, Cambridge. You will conduct high-quality clinical and laboratory studie...Read More>>.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring activities align with study protocols, GCP, SOPs and regulatory requirements.You will develop relationships with cli...Read More>>.

AbbVie in Maidenhead seeks a Field-based CRA to advance AbbVie's clinical pipeline by ensuring high-quality site conduct and data integrity across studies. You will partner with study teams, internal R&D stakeholders, investigators and site staff...Read More>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol trai...Read More>>.

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives acr...Read More>>.

Ready to take ownership of early-phase clinical trials while gaining the variety, autonomy and visibility that larger CROs often can't offer?Join a boutique, early-phase CRO partnering with innovative biotechnology companies across a varied...Read More>>.

Norwich Clinical Trials Unit at the University of East Anglia is seeking a Research Associate to support high-quality clinical statistics delivery within the Norwich Clinical Trials Unit.The role involves working with a Senior Statistician...Read More>>.

IQVIA LLC in the United Kingdom is seeking a site management/monitoring professional to oversee the progress of assigned studies, including regulatory submissions, recruitment, CRF completion and data query resolution. The role requires coordinati...Read More>>.

IQVIA UK is seeking an experienced Clinical Research Associate for the South West England region. The role involves on-site monitoring visits, protocol training, and collaboration with study teams to ensure regulatory compliance and data integrity...Read More>>.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoo...Read More>>.

Clinical Operations (multi-sponsor)Our team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Onc...Read More>>.

WhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study (PSV), site initiation (SIV), interim monitoring (IMV), and close-out (COV)) and complete site visit deliverables with quality and...Read More>>.

CTI is seeking a Clinical Research Associate with 3–5 years of experience to serve as the primary CTI contact for assigned study sites and conduct routine site visits, ensuring quality and adherence to regulatory standards.The role involv...Read More>>.

Research Associate (Behaviour Change & Co-production) - Neuadd Meirionnydd, CardiffResearch Associate (Behaviour Change and Co-production)Centre for Trials Research (CTR)College of Biom...Read More>>.

Research Associate - Tower Building, CardiffResearch AssociateCardiff Babylab is looking for a full-time Research Associate to join our team which is funded by...Read More>>.

Research Associate (Qualitative) - 2 Posts - Neuadd Meirionnydd, CardiffResearch Associate (Qualitative) - 2 PostsCentre for Trials Research (CTR)College of Biomedical & Life SciencesTh...Read More>>.