Senior Clinical Trial Associate - Shanghai, Shanghai

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a ...

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials. · Typical duties will include supporting other members of the local study team, · collecting data required for regulatory submissions, · document tracking contracts financ ...

At · Emerald Clinical Trials · , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutic ...

We are currently seeking a Senior Clinical Trial Assistant (CTA) to join our diverse and dynamic team. · Providing administrative support for clinical trials. · Assisting in the preparation and submission of regulatory documents. · ...

Job Overview · Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. · Essential Functions · Assist Clinical Research Associates (CRAs) and Reg ...

This position involves participating in all stages of clinical trial development including feasibility assessments protocol design CRF design investigational site selection generation of clinical study reports. · ...

We are currently seeking a Clinical Associate to join our diverse and dynamic team at ICON plc. As a Clinical Associate at ICON you will play a pivotal role in supporting the design implementation and management of clinical trials contributing to the advancement of innovative tre ...

The Document Management Associate will provide support for Trial Master File activities to clinical teams. · Manage Trial Master Files (TMF), both electronic and paper format according to project requirements. · Set up receive track and maintain electronic or paper TMFs according ...

Thispositionisresponsibleforassistingclinicalresearchteamsineffectivelyconductingclinicalresearchstudiesbyprovidingadministrationandprojecttracking. · ...

The Project Manager is responsible for the planning and management of all contracted responsibilities for assigned projects. Leads and oversees the execution of clinical projects in accordance with local regulation, ICH GCP guidelines, Novotech/client SOPs and the Project Agreeme ...

Clinical Project Manager insourcing to one of the global MNC. Manage study timelines, budgets and quality targets. · ...

Senior Statistical ProgrammerWe are seeking an experienced SAS programmer to join our team... · ...

This is an office-based medical role with the aim of providing high-quality scientific advice to Chiesi's internal functions regarding company products and associated disease areas. · Owner of national Advisory board and its plan/execution · Analyze scientific & clinical care gap ...

The Study Manager will be the technical expert for study management systems and processes and champion the implementation and use of harmonized, consistent processes. · ...

Lead and guide junior application engineer to achieve AE value in technical support responsibilities. · ...

We are a global healthcare leader headquartered in Indianapolis, Indiana. We unite caring with discovery to make life better for people around the world. · ...

Band · Level 4Job Description Summary · To lead Patient Safety operational processes at the Country Organization ensuring compliance with Novartis global and local procedures, national and international regulations/ standards/ guidelines for vigilance of Novartis group approved, ...

Summary · To lead Patient Safety operational processes at the Country Organization ensuring compliance with Novartis global and local procedures, national and international regulations/ standards/ guidelines for vigilance of Novartis group approved, marketed and investigational p ...

+As an Medical Science Liaison for Organon LLC you will engage in non-promotional exchange of medical information with healthcare professionals. · Develop SLs list for regions to be covered. · Organize medical exchange activities including journal clubs. · ...

The Senior Scientist will be responsible for developing and reviewing documents, preparing and conducting trainings, supporting application development, participating in independent reviewer selection and performance monitoring. The ideal candidate should have experience working ...