Who we are Worldwide Clinical Trials (Worldwide), a leading global contract ... to the successful conduct a clinical research project. Ability to mentor ... least 5 years experience in clinical research and at least 2 ...
... primary, client-facing clinical leader for Quartet’s Care Connections, ... 5+ years of clinical experience 3+ years in some combination of clinical program design across different lines ... maintaining a part time clinical practice Experience working in or ...
... excel in delivering high-quality clinical and regulatory writing, from the ... the broader objectives of our clinical development program. Here’s What You’ll ... processes for writing and reviewing clinical and regulatory documents. Document Updates: ...
... 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 ...
... 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 ...
... 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 ...