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The CTOS is accountable for supporting the oversight of trial supplies, documentation, submissions, co-ordination of communication, and the management of complex technical systems to manage clinical ...
We're currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an ...
We are seeking adventurous souls to join our team as a Clinical Trials Manager! If you're passionate about making a difference in healthcare and thrive in dynamic environments, this is the ...
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Lead the clinical trial team * Plan, deliver and manage clinical trial activities * Liaise with the clinical trial team members * Management of global vendors * Point of contact with sponsor on ...
Life Sciences Recruitment is pleased to confirm that we are working with our global, fast-growing clinical trial supply (CTS) client, to hire a Project Manager to join their Unlicensed Medicines ...
Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: • Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with ...
... clinical trial submissions managed by other stakeholders such as IB, Protocols. * the approved company CTA processes are followed within agreed timelines. * understanding of CTR process and ...
... clinically differentiated solutions that deliver measurably better patient outcomes and more ... Manage reprocessing of our Rental/Loan/Trial fleet of devices. * Assist with spare part warehouse ...
The Senior Clinical Trial Manager works within the clinical trial team to provide regional trial oversight and ensures deliverables are met in terms of quality, compliance, and timing. This role may work collaboratively on one trial or across several trials to support clinical operations activiti...
We are seeking adventurous souls to join our team as a Clinical Trials Manager!. Experience the thrill of managing global clinical studies and shaping the future of medicine. Lead regional management efforts on Phase Ib-III clinical studies. Previous experience in clinical research or study manag...
Title: Clinical Trial Manager - Global Pharma - Complex Trials. We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. Provides regional management of global PIb-III studies managed by Clinical Pr...
Represent area regulatory in clinical trial planning meetings and provide strategic and operational support for Company CTAs for Company sponsored clinical trial Primary interface to and from affiliate personnel in over 60 countries. We’re currently recruiting for a Regulatory Clinical Trial Stra...
To perform the role of Clinical Trial Manager (CTM) on assigned trials on a 12 month contract. Accountable for the operational management of the local (UK & Ireland) component of a clinical trial. Leads local trial team to ensure integrity of trial conduct and assurance of patient safety. Require...
Previous clinical study management/clinical project management as a study manager/clinical project manager. ICON: Global Clinical Trial Manager ICON United Kingdom Remote. Collaborating with Regional Clinical Trial Manager to ensure country level study delivery aligned with global delivery plans....
Works with Clinical Program Managers to manage regional component of Virology clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. The successful candidate will be a member of the Global Study team overseen by a Clinical Pr...
Title: Clinical Trials Manager. The successful candidate will be a member of the Global Study team overseen by a Clinical Program Manager. Provides regional management of studies managed by Clinical Program Manager. The CTM role will involve regional management on clinical studies, with a strong ...
Work with Clinical Program Managers to manage regional Virology clinical trials. Manage regional Phase Ib-III clinical studies in the EMEA region. Draft and coordinate review of study documents like protocols, case report forms, and clinical study reports. ...