Cra jobs

 ...communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals / targets. May act as primary liaison with project site personnel, or in collaboration with... 

Thermo Fisher Scientific seeks Clinical Research Associates to join its PPD Functional Service Provider division in the UK on a remote basis. The role involves clinical monitoring across multinational projects within a CRO environment, supporting pharmaceutical trials and research...

IQVIA seeks a Senior Clinical Research Associate to conduct site qualification, monitoring, and close-out activities for clinical trials across multiple therapeutic areas. The role combines embedded sponsor-level exposure with IQVIA's global infrastructure, requiring extensive...

IQVIA seeks a Clinical Research Associate II to monitor Phase 3b and Phase 4 studies across UK and Ireland sites. The role involves conducting site visits, managing recruitment, ensuring regulatory compliance, and coordinating with study teams to maintain protocol integrity...

 ...We're delighted to invite UCL Economics students to an exclusive office visit at Charles River Associates (CRA) on Tuesday, 24th November 2026 . During the visit, you'll meet colleagues from our Antitrust & Competition practice, explore our London office, and gain first... 

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting...

 ...team is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The CRA will cover sites across UK & Ireland, with 6-7 site visits per month. Why join IQVIA? Community – collaborate with diverse teams... 

 ...has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development! Responsibilities Perform site monitoring... 

JOB DESCRIPTION Work Schedule Other Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling...

IQVIA Biotech seeks a Senior Clinical Research Associate to conduct site monitoring for clinical trials with emerging biotech partners. The role involves managing study sites, ensuring regulatory compliance, tracking enrollment and data quality, and supporting protocol implementation...

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA’s Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Genuine career development opportunities to grow as we grow...

 ...CRA II/Senior CRA - Early Phase ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are... 

 ...investigational product inventory, and serve as primary contact between sponsor and investigators Requirements Minimum 2 years experience as a CRA Clinical trial monitoring and/or coordination experience Oncology experience required Strong knowledge of clinical research... 

 ...position cannot offer visa sponsorship, candidates must hold right to work in UK & Ireland. Build Your Future with IQVIA As a Senior CRA at IQVIA, you'll apply your clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. You'll... 

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) ...

 ...Fortrea seeks a CRA I or II for a fixed-term post-market surveillance study role based in Maidenhead. The position involves monitoring investigator sites across Northern England, managing site relationships, and ensuring compliance with regulatory standards and data quality... 

Senior CRA - 5+ years of exp needed At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a... 

 ...Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements. Responsibilities Participates in the... 

Senior Clinical Research Associate at ICON overseeing clinical trial monitoring and site management in a sponsor-dedicated model. Requires 5+ years of experience managing multiple sites while ensuring protocol adherence, regulatory compliance, and data integrity across global...

IQVIA Biotech seeks a Clinical Research Associate 2 to conduct site monitoring visits, manage study progress, and ensure regulatory compliance for clinical trials. The role involves working with biotech and biopharma sponsors in a dynamic, fast-paced environment across multiple...

IQVIA seeks an experienced Senior Clinical Research Associate for sponsor-dedicated monitoring in the UK. The role involves conducting site visits, managing study progress, ensuring protocol adherence, and maintaining regulatory documentation across assigned clinical trials...

IQVIA is hiring Clinical Research Associates to conduct site monitoring, manage study operations, and ensure protocol compliance across UK locations. The role involves site visits, recruitment oversight, data quality assessment, and regulatory documentation within a sponsor...

 ...to join our team in the UK across a range of locations. **Competitive sign-on bonus considered for qualified candidates** The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to... 

Thermo Fisher Scientific (PPD) seeks experienced Clinical Research Associates to support clinical trial operations across UK locations. The role involves site monitoring, protocol compliance oversight, data integrity verification, and coordination between investigative sites...

 ...collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a UK home-based CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality monitoring... 

 ...Sr CRA At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where... 

ICON seeks a Clinical Research Associate to deliver clinical trial monitoring in a UK home-based role. The position involves coordinating study setup and monitoring activities, managing sponsor queries, and ensuring regulatory compliance across clinical programmes. Responsibilities...

 ...degree in Life Sciences or equivalent relevant experience At least 1 year of independent clinical trial monitoring experience as a CRA Understanding of ICH-GCP guidelines and clinical trial processes Knowledge of or interest in unblinded monitoring and investigational... 

 ...Fortrea seeks a CRA II to conduct site monitoring visits and manage clinical trial activities across UK locations. The role involves ensuring protocol compliance, data integrity, and regulatory adherence while supporting study initiation through closeout phases. Responsibilities... 

Are you looking to grow your career in clinical research? Fortrea is hiring a CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in the Midlands, offering an exciting chance to work on diverse studies while ensuring compliance with...