Company: Pharmaceutical Research Associates, Inc

Overview As a Global Study Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities The Global Study Manager provides input to the overall operational trial(s) implementation, manages trial(s) timelines, budget, feasibility, country identification and sites selection, enhanced patient recruitment, functions as the primary liaison for [...]Read More... from Global Clinical Trial Manager See details

Overview As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will lead, manage, and coordinate all internal and external writing activities associated with the preparation, compilation, and submission of applications to regulatory authorities globally. Responsibilities What you will be doing: Develop [...]Read More... from Principal Medical Writer See details

Overview Do you have experience in creating data transfer agreements and data mapping? Are you looking to work with Electronic Health Records and be involved in a new exciting role? Responsibilities What you will be doing: Provides specialised expertise in the collection of electronic data (non-CRF data). Supports the development of data transfer agreements. Liaises [...]Read More... from Senior Clinical System Designer See details

Overview We are hiring! Contract and Costings Managers (working on non-Oncology clinical trials), either from home or at our client’s Luton office. It is a very exciting time at ICON – ICON plc is a world-leading healthcare intelligence and clinical research organisation. With our patients at the centre of all that we do, we help [...]Read More... from Study Contracts Manager – Biopharma Division See details

Overview Job title: Senior Clinical Trial Manager – 14 month assignment (potential to be extended or reassigned within ICON) Location: United Kingdom – fully remote Sponsor dedicated As a CTM, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities Working fully embedded within an ever-expanding program [...]Read More... from Senior Clinical Trial Manager – UK/IRE See details

Overview 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 of drugs and devices [...]Read More... from Pharmacovigilance Associate See details

Overview As a Sr SDTM Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities What you will be doing: Interact with vendors to receive CRF & external data. Review data transfer specs to ensure data is in a form we can use (SAS compliant variable [...]Read More... from Clinical Programmer – SDTM See details

Overview We are currently seeking a Clinical System Designer to join our diverse and dynamic team. As a Clinical System Designer at ICON, you will play a critical role in designing and optimizing clinical systems that support the efficient management of clinical trials. You will contribute to the advancement of innovative therapies by ensuring that [...]Read More... from Clinical System Designer See details

Overview An additional UK home-based Oncology Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region. You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work [...]Read More... from UK Clinical Project Manager See details

Overview Job title – Senior Clinical Research Associate – Hematology experience required Location – UK, nationwide travel Fully sponsor dedicated As a SCRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities Your ultimate responsibility as a SCRA includes ensuring trial sites are inspection ready through [...]Read More... from Senior CRA – Hematology experience required See details