... to pre- and post-market clinical investigations, as well as all ... to and learning from global clinical investigation submission and strategy experiences. ... or global regulations related to clinical investigations. You have strong time ...
... to pre- and post-market clinical investigations, as well as all ... to and learning from global clinical investigation submission and strategy experiences. ... or global regulations related to clinical investigations. You have strong time ...
... and enrollment planning for global clinical trials. If you are an individual with a clinical background and expertise in clinical research, please review the following ... ; Fluency in English language; Some clinical research experience is beneficial; and ...
... Activation and Maintenance team, within Clinical Operations. This role will be ... strategic regulatory advice to support clinical trial submissions. Medpace specialises in supporting ... on complex and challenging trials, often involving new technologies and ...
... globally Assuring adherence to Good Clinical Practices, investigator integrity, and compliance ... Min 2 years experience as Clinical Project Manager within a CRO Experience in commercial studies Experience in clinical studies phase II-III Fluent ...
... Around 1-3 years of clinical trials experience. Preferably at least 1- ... in vendor management, proposal development, clinical trial operations, or business development working ...
... with ICH-GxP principles and clinical trial regulations to be based in ... -out the lifecycle of the clinical trial. Partner with operational delivery teams ... proud to be a leading Clinical Research Organization with colleagues across ...
... are well-prepared to commence clinical trials for investigational products at their ... but not required. Experience of Clinical Trial operations and meeting regulatory guidelines Proficiency in a clinical research environment, with specific experience ...
... quality to ensure patients on Clinical trials have access to safe and ... and on-going management of clinical trial agreements (CTA) with investigative sites and investigators. Works cross functionally with Clinical and RSU Team in support ...
... complete, high quality and reliable clinical trial data for regulatory approval and ... in practice. Understanding of clinical drug development process Previous experience ... advanced analytics, technology solutions and clinical research services to the life ...