Clinical Study Administrator

Job OverviewThe Senior Study Manager will lead cross-functional clinical trial teams, guiding planning and management of assigned clinical studies from start to finish. This role is accountable for proactive operational planning with effective contingencies and risk management.Key ResponsibilitiesExecute and deliver clinical studies, guiding planning and...

We are seeking a detail-oriented and organized Project Manager to oversee the preparation of Clinical Study Reports (CSRs). This role involves authoring CSR appendices, compiling clinical study data, and tracking and coordinating all appendices. The successful candidate will work closely with various study team members to ensure each CSR appendix is...

Job SummaryThe Clinical Research Study Leader will be responsible for leading the development and execution of patient recruitment and retention strategies for global clinical trials. This role will involve managing large-scale campaigns, collaborating with vendors, and analyzing recruitment reports to optimize strategy and tactics.Key...

As a Clinical Project Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The CPA will interact on a global scale within the study team and clinical team. The CPA sphere of influence and communication will include the Global Clinical Lead, the Clinical Project Manager,...

Study Support Assistant At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Clinical Research Associate Job SummaryAbout UsENGINEERINGUK is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.Job ResponsibilitiesWe are seeking a Clinical Research Associate to join our team in the UK. The successful candidate will be responsible...

Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. This role offers hybrid working, with 2-3 days on site...

Home based in the United Kingdom, we are seeking a highly skilled Senior Toxicology Study Manager to partner with our global pharmaceutical client. This is an exciting opportunity for you to join their team and contribute to the development of innovative medicines.About the RoleIn this fully home-based position, you will be responsible for leading study...

Job Summary:As an Administrative Assistant - Clinical Trials, you will be supporting daily operations to ensure accurate Trial Master File delivery, updating clinical documents, and managing data flow. You will work closely with the clinical team to prepare, handle, distribute, file, and archive clinical documentation and reports according to scope of work...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Job OverviewAt Pharmiweb, we are seeking a highly organized and detail-oriented Clinical Trials Assistant to support our clinical research team. The successful candidate will be responsible for performing daily administrative activities, including updating and maintaining clinical documents and systems, and assisting with the preparation and handling of...

UK Biobank is a leading biomedical research organization that seeks to hire a Clinical Research Radiographer to play a key role in the Imaging Enhancement Study. This fixed-term contract position is based in Reading and offers a unique opportunity for a qualified Radiographer to contribute to groundbreaking research. As a Radiography Team Member, you will be...

**Company Overview**At Intuitive, we pioneer minimally invasive care. Our mission is to empower physicians to heal without constraints through intelligent technology and ingenuity.We are united behind our vision of making a difference in the world of healthcare. With over 25 years of experience working with hospitals and care teams worldwide, we strive to...

Job SummaryThe Patient Recruitment Lead will support the development and execution of Patient Recruitment and Retention strategies and tactics appropriate to the awarded study needs and in alignment with the Sponsor requirements.Key ResponsibilitiesDevelop and execute patient recruitment and retention activities on global, multi-tactic campaignsManage...

Job DescriptionThis Study Start-Up Associate Manager position plays a vital role in the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.You will be responsible for managing and maintaining comprehensive and accurate records of regulatory submissions,...

Study Start Up Associate / Contract Specialist At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an...

Job PurposeThe Global Clinical Trial Manager is responsible for leading cross-functional clinical trial teams, guiding planning and management of assigned clinical studies end-to-end to achieve objectives. This role requires proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the clinical trial team....

Job PurposeThe Senior Clinical Research Leader is responsible for leading cross-functional clinical trial teams, guiding planning and management of assigned clinical studies to achieve objectives. This role requires proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the team.Key...

Job PurposeThe Global Clinical Trial Leader is responsible for guiding the planning and management of clinical studies from start to finish. This involves proactive, iterative operational planning with effective contingencies and embedded risk management mindset. The role oversees budget and people allocation within assigned studies and contributes to...