Overview As Biostatistician at CRCTU, you will provide statistical expertise for the design, analysis and reporting of cancer clinical trials. You will collaborate with clinical investigators and contribute to protocols, SAPs, interim analy...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 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 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 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 In this role you will join the Clinical Trial Management team to oversee and streamline global trial activities. You will work closely with project coordinators and managers to ensure timely, accurate delivery and documentation. Yo...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 will support the Clinical Trial Management team in London, applying your PhD-level research skills to clinical project administration. You will collaborate with project coordinators, clinical trial managers, sites,...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 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>>.

Medpace is seeking a Medical Monitor Hepatology to join their team in London. The role requires providing medical, scientific, and strategic leadership for clinical trials. The Monitor will act as the internal medical expert and contribute to the...Read More>>.

Medpace, Inc. is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Stirling. The role supports daily regulatory submissions activities, timelines, and documentation throughout the trial ma...Read More>>.

Join IQVIA on our mission to accelerate innovation for a healthier world! We are seeking a Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team. This position requires candidates able to commit to ad-hoc travel sponsor's office i...Read More>>.

IQVIA in Maidenhead, Berkshire, is seeking a Clinical Trials Assistant to support the cFSP sponsor-dedicated team. The role involves maintaining trial master files, preparing and filing documents, and assisting with trial supply logistics.T...Read More>>.

Johnson & Johnson Innovative Medicine in the United Kingdom seeks a Manager, Trial Delivery Management to oversee study delivery across multiple countries, ensuring alignment with feasibility strategy and risk reviews. The role includes vendor ove...Read More>>.

Our client requires an experienced Pharmacy Technician with Clinical Trials experience to start as soon as possible.This Hospital offers onsite parking.Key Skills Required:Clinical Trials ExperienceNHS Hospi...Read More>>.

The Locum Agency is seeking an experienced Pharmacy Technician with Clinical Trials experience to work with an NHS hospital client in England. The role requires NHS hospital experience and GPhC registration.The hospital offers onsite parkin...Read More>>.

Clerkenwell Health is seeking an Office Assistant to provide front-of-house and general office support at our London sites, including Marylebone/Baker Street. You will welcome trial participants, manage enquiries, and help keep the site organised...Read More>>.

Job Title: Clinical Trials Specimen Management TechnicianDepartment: Specimen ProcessingLocation: Onsite, York, UKHours Per Week: 37.5Schedule: Monday - Friday, 9:00 AM - 5:00 PM OR Tuesday - Saturday, 8:00...Read More>>.

Rochester Regional Health is seeking a Clinical Trials Specimen Management Technician I to perform daily CTSM laboratory operations on onsite shifts in York. You will process specimens, carry out QC checks, and prepare samples for shipment while u...Read More>>.

Richmond Pharmacology in London Bridge is seeking a Contracts Coordinator to lead the financial management of clinical trial projects, focusing on contract management, budgeting, and vendor coordination to ensure projects run on time and within bu...Read More>>.

Rochester Regional Health in York, UK, is seeking a Clinical Trials Specimen Management Technician I to support daily CTSM laboratory operations. The role involves specimen receipt, QC checks, data entry, sample preparation for shipment, and stora...Read More>>.

Cardiff University is seeking an experienced Administrator to provide comprehensive professional administrative support to a project in the Department of Child Health, Heath Campus. The role requires proficiency in MS Office, ability to establish...Read More>>.

The Barberry, National Centre for Mental Health, Birmingham, is recruiting a Band 6 Clinical Trials Research Nurse to support the Lead Research Nurse in delivering high-quality trials across mood disorders, epilepsy, psychosis and other mental hea...Read More>>.

Oxford Health is seeking a proactive Research Delivery Team Leader to bridge clinical excellence with academic innovation. You will act as the link between Oxford Health and the University Department of Psychiatry, driving research growth and ensu...Read More>>.

hVIVO is seeking a Research Nurse to support daily planning and execution in our viral challenge unit in Canary Wharf (E14) and Outpatient unit (E1) on a one year fixed-term contract. Start ASAP.You will ensure safety, assist with workload...Read More>>.

Medpace is hosting a Recruitment Event in Central London for Medical Doctors with MBBS seeking to switch into the Clinical Trials industry. The Associate Clinical Trial Manager (aCTM) will join the London Clinical Trial Management team and work wi...Read More>>.

Job Summary Medpace is delighted to host a Recruitment Event tailored to Medical Doctor's - candidates with a Bachelor of Medicine, Bachelor of Surgery qualification. This is a rare and exciting opportunity for Med...Read More>>.

Fortrea's Clinical Research Unit in Leeds is seeking an enthusiastic, customer-focused individual to handle inbound and outbound calls with potential study participants. The role involves screening participants, collecting medical history, and boo...Read More>>.

The Institute of Cancer Research, together with the Royal Marsden NHS Foundation Trust, invites applications for a Clinical Research Fellow in Urological Cancer (STAMPEDE2). The post contributes to clinical and translational research, with focus o...Read More>>.

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in line with the study protocol, GCP, and Velocity SOPs. You will coordinate start-up activities, vendor management, recruitment, d...Read More>>.