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 global non-interventional studies as a Senior Lead CRA, guiding cross-country teams to ensure high-quality site management and compliance. You collaborate with Sponsors, PMs, and regulators to advance study s...Read More>>.

Overview In this role you support the execution of interventional studies as a Clinical Research Associate within IQVIA's sponsor-dedicated team. You will conduct on-site monitoring and ensure compliance with GCP/ICH while collaborating wit...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>>.

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>>.

Get AI-powered advice on this job and more exclusive features.Direct message the job poster from EPM ScientificConsultant at EPM Scientific | Permanent SolutionsWe're currently partnering with a leading international pharmac...Read More>>.

Join to apply for the Senior Clinical Research Associate role at TFS HealthScience3 weeks ago Be among the first 25 applicantsJoin to apply for the Senior Clinical Research Associate...Read More>>.

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach...Read More>>.

Headlands Research is seeking an experienced Nurse Practitioner or Physician Assistant to support clinical trials at the onsite site in Chesterfield, MO. The role involves patient care across gastroenterology, neurology, vaccines, and general inte...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>>.

RELX INC's Cell Reports Medicine seeks a Senior Scientific Editor to shape the journal's scientific direction, oversee the peer review process, and collaborate with authors and reviewers across translational and clinical research.Candidates...Read More>>.

Research Associate - Community Engagement & Participatory Design (Milton Keynes, ENG, GB, MK7 6AA)Change your career, change livesThe Open University is the UK&...Read More>>.

Postdoctoral Research Associate - Oncolytic Clostridia as Prostate Cancer Therapeutics (Milton Keynes, ENG, GB, MK7 6AA)Change your career, change livesThe Open...Read More>>.

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory complian...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>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor and manage study sites, ensuring adherence to protocol, GCP/ICH guidelines, and regulatory requirements. The role involves site visits, recruitment support, trai...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>>.

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>>.

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>>.

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>>.

R&D Partners is seeking a Clinical Research Associate to coordinate and oversee clinical studies in the UK. You will act as the primary contact for study sites, support site activation, and collaborate with cross-functional teams to ensure success...Read More>>.

Are you ready to drive the future of clinical research? Looking to be in the heart of a company where precision meets purpose? R&D Partners is seeking a Clinical Research Associate to join our team. In this role, you will coordinate and ove...Read More>>.

The Research Fellow will play a pivotal role in advancing psychological and multi-disciplinary research, audit and quality improvement (QI) within the Children and Young People's Gender Service (CYPGS) and Psychological Health Services (PHS). Work...Read More>>.

An exciting opportunity has arisen for a Band 6 Clinical Research Nurse post within the GI and Lymphoma Unit. The post holder will be working in the GI and Lymphoma unit Unit at the Royal Marsden NHS Foundation Trust based at Sutton. We are a high...Read More>>.

A leading clinical research organisation is looking for a Registered Nurse to support patient recruitment and study delivery at a busy clinical research site. This role will play a key part in the day-to-day running of clinical trials, ensu...Read More>>.

Main duties of the jobAn exciting opportunity has arisen for a Nurse to join the Research and Development team. The Research Nurse will be responsible for wide variety of studies covering many disease sites. This post will also develop yo...Read More>>.

Help shape the future of healthcare through research. We're looking for a motivated and organised individual to support the delivery of clinical research studies. You'll work closely with research teams, healthcare professionals and patients to he...Read More>>.

Imperial College Healthcare NHS Trust in London seeks an experienced chemotherapy nurse to join a multidisciplinary team delivering systemic anti-cancer therapies within a clinical research setting.The post holder will recruit and assess pa...Read More>>.

This is an exciting role which will offer candidates the opportunity to continue to work in a clinical environment whilst also developing their research skills. The post holder will be part of a multidisciplinary team including experienced clinica...Read More>>.

The Betsi Cadwaladr University Health Board invites applications for a Clinical Research Officer Band 5 to join the Health and Care Research Wales Research and Development team in North Wales. The post aims to boost patient participation in clinic...Read More>>.

Job Overview An exciting opportunity has arisen for a Clinical Research Officer Band 5 to work as part of the Health and Care Research Wales Research and Development team in the BCUHB. The purpose of this post is to increase the number of...Read More>>.

Careers Site Advertising End DateAdvertising End Date: Careers Site Advertising End DateAdvertising End Date: 25 Oct 2026 Internal Advertising End DateInternal Advertising End Date:...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring compliant conduct, documentation and reporting in line with GCP, SOPs, and regulatory requirements.You will develop...Read More>>.