Overview In this role you will support clinical trial management activities within the Stirling-based Clinical Trial Management team. You will work closely with project coordinators and trial managers to ensure timely, accurate delivery of...Read More>>.

Overview In this role you drive the day-to-day operations of clinical trials, ensuring compliance and timely delivery within ICH/GCP guidelines. You will serve as the primary Sponsor contact for operational issues and oversee cross-function...Read More>>.

Overview In this role you help grow our clinical trial footprint by supporting and expanding site relationships across the UK and Hungary. You’ll collaborate with the Clinical Operations team to run feasibility assessments, select sites,...Read More>>.

Overview In this role you will strengthen and manage relationships with trial sites as part of Medpace’s Clinical Operations team. You will shape feasibility strategies for the UK and Italy, support site selection and study start-up, and...Read More>>.

Overview In this role you will join the Clinical Trial Management team to support global study activities and timelines. As an early-career professional with a PhD, you will transfer analytical and academic skills into clinical project admi...Read More>>.

Overview In this role you will support the rapid growth of clinical activities by managing site relationships and driving feasibility efforts in the UK and Hungary. You will work within the Clinical Operations team to shape site networks, e...Read More>>.

Overview As a Clinical Trial Manager at Medpace, you oversee day-to-day operations of CNS-focused clinical studies, ensuring adherence to ICH/GCP and regulations. You serve as the primary sponsor contact, guiding a cross-functional team and...Read More>>.

Overview In this role you will lead day-to-day operational management of clinical trials in the London office, ensuring compliance with ICH/GCP and applicable regulations. You will act as the primary sponsor contact for operational issues a...Read More>>.

Overview In this role you will lead the development and validation of molecular, virology, microbiology and immunology assays to support hVIVO’s business and client projects. You will manage multiple studies, mentor junior staff, and coll...Read More>>.

Overview In this role you will join Medpace’s Clinical Trial Management team to support end-to-end trial management for radiopharmaceuticals-related studies. You will collaborate with Project Coordinators, Clinical Trial Managers, and spo...Read More>>.

Overview In this role you will join Medpace’s Clinical Trial Management team to support global trial delivery. You’ll work closely with project coordinators and Clinical Trial Managers to apply analytical and academic skills to clinical...Read More>>.

Overview In this role you will oversee day-to-day operations of clinical studies in Leuven, Belgium, applying ICH/GCP standards within a CRO context. You will serve as the main sponsor contact for operational issues and study deliverables,...Read More>>.

Overview In this role you support the Clinical Trial Management team in Stirling, applying academic expertise to clinical project administration. You will collaborate with project coordinators and managers on global study activities, ensuri...Read More>>.

Overview As a Clinical Trial Manager at Medpace in London, you drive day-to-day trial operations within a global CRO framework. You will act as the primary sponsor contact for operational issues and ensure study deliverables meet ICH/GCP st...Read More>>.

Overview In this role you will lead global clinical trials from design to study reporting, ensuring delivery on time, budget and quality. You will work with cross-functional teams, external partners and local regulators to drive successful...Read More>>.

Overview In this role you drive the day-to-day delivery of clinical trial operations in London within Medpace’s Clinical Trial Management Group. You leverage your therapeutic expertise (Cardiovascular/Endocrine/Metabolic) while ensuring c...Read More>>.

Overview In this role you will manage day-to-day operations of clinical projects within Medpace's Clinical Trial Management Group in the UK, aligning with ICH/GCP standards. You work closely with cross-functional teams and act as the primar...Read More>>.

Overview In this role you join Medpace’s Clinical Operations team in London to strengthen site networks and drive feasibility for UK and Hungary. You will support pre-award and post-award activities, build strategic site relationships, an...Read More>>.

Overview In this role you support global clinical trial management, collaborating with Project Coordinators and Clinical Trial Managers to advance study activities. You will apply analytical and academic skills to practical trial administra...Read More>>.

Overview In this role you drive the ongoing development of Cortellis Clinical Trials Intelligence within the Competitive Intelligence team, serving as the clinical expert to align product output with drug development needs. You will support...Read More>>.

Overview In this role you will join Medpace’s London Clinical Trial Management team to oversee and support global clinical trial activities. You will work closely with project coordinators and clinical trial managers to ensure timely, acc...Read More>>.

Overview As an Associate Clinical Trial Manager, you will support global clinical trial activities within Medpace’s Clinical Trial Management team, translating academic research skills into practical project administration. You’ll colla...Read More>>.

Overview In this role you will help safeguard the integrity of clinical trial data by reviewing rater-administered scales and guiding methodology and scoring. You will work with raters through live feedback and calibration sessions, support...Read More>>.

Overview In this role you join Medpace’s Clinical Trial Management team to support global studies. You apply analytical and academic training to clinical project administration and oversight, collaborating with project coordinators and cl...Read More>>.

Overview In this role you will join the London Clinical Trial Management team to support global study delivery. You will work with Project Coordinators and Clinical Trial Managers to manage study activities and documentation. The position o...Read More>>.

Overview In this role you support the operational aspects of planning, start-up, conduct, and close-out of clinical studies, collaborating with Neurocrine, CROs, and investigator sites to ensure compliant, high-quality trial execution. You...Read More>>.

Overview In this role, you will support and strengthen site partnerships across the UK and Hungary to enable efficient feasibility and study start-up. You’ll work closely with the Clinical Operations team to identify new business opportun...Read More>>.

Overview In this role you will contribute to the management of large clinical trial protocols within the CRCTU, ensuring ethical and regulatory compliance and high-quality data. You will work across trial sites, coordinate governance, and h...Read More>>.

Overview In this role you will oversee the CRCTU's Business Support Team, ensuring robust HR, financial, and administrative services to support strategic aims. You will contribute to planning, reporting, and resource management within a lar...Read More>>.

Overview In this role you will lead and coordinate operational activities for assigned clinical studies, both domestically and globally. You will manage CROs and CSPs, ensuring studies comply with FDA, EU, ICH, and SOPs, while partnering wi...Read More>>.

Overview In this role you will be a highly specialized clinical trials pharmacist focusing on oncology and haematology. You will work within the clinical trials pharmacy team while maintaining and developing oncology clinical expertise alon...Read More>>.

IQVIA is seeking a Clinical Independent Rater who speaks Romanian to support clinical trials on a remote basis. The role involves reviewing patient assessments, scoring scales, and participating in calibration discussions with raters.This i...Read More>>.

ACM Global Laboratories, Inc. is seeking a Proposals Analyst Pre Award to support clinical trials business development. The role focuses on pricing strategy, RFP review, and cross-functional collaboration with global affiliates.The position...Read More>>.

East of England Community Health and Care NHS Trust is seeking a NMC Registered Nurse or Midwife to lead the delivery of NIHR Research Delivery Network (RDN) Portfolio studies across the RRDN region. The post involves flexible working with multipl...Read More>>.

University Hospitals Of Leicester NHS Trust is seeking a Senior Agile Research Delivery Team Nurse/Midwife/Allied Health Professional to join the Agile Research Delivery Team. The role requires flexible, autonomous working across disciplines and r...Read More>>.

PSI is seeking a Specialist Talent Acquisition professional for a one-year remote contract within the UK. You will lead end-to-end recruitment across Europe, delivering an outstanding candidate and hiring manager experience while partnering with e...Read More>>.

For questions about this job, contact: Name: Amy Humphries Position: Senior Research Nurse Email: amyhumphries@nhs.net Job Summary The Oncology Research Delivery Team is a highly skilled, patient-focused & dedicated to bringing inn...Read More>>.

Novartis Pharmaceuticals UK Ltd. is seeking a Clinical Research Associate to monitor Phase I–IV studies across London/UK. In this site-facing role, you will manage trial sites, ensure regulatory compliance, and build strong site partnerships....Read More>>.

Fulfil your potential in hospitals that make history: Charing Cross, Hammersmith, St Mary’s, Queen Charlotte’s & Chelsea and Western Eye. With five world-renowned hospitals, Imperial College Healthcare NHS Trust is full of...Read More>>.

The Christie NHS Foundation Trust in Manchester is seeking an experienced nurse to join the Clinical Research Facility (CRF) as a key member of the team. You will support the Unit Manager, lead the nursing team, and help implement service changes...Read More>>.

IQVIA is seeking a Country-level Site Activation professional to manage activation tasks for UK sites, working remotely with the SAM and project team. You will ensure regulatory readiness, maintain study documents, and monitor timelines in line wi...Read More>>.

An opportunity has arisen to appoint a Band-6 Research Midwife/Nurse to work within the WHRC. The postholder will be responsible for supporting the day-to-day delivery of clinical research, including consenting participants, collecting samples, an...Read More>>.