Clinical Study Operations Manager

Study Start-Up ManagerAs a Study Start-Up Manager, you will be responsible for ensuring the successful start-up of clinical studies in compliance with Client procedures and guidelines.Key responsibilities include:Providing regular updates to Line Managers on study and planned study milestonesSupporting Study Management and Monitoring in different...

Pfizer Medical and Safety TeamWe are seeking a highly skilled Clinical Study Operations Manager to join our team. As a key member of our medical team, you will play a crucial role in connecting evidence-based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.Key Responsibilities:Manage clinical studies...

Job Summary: We are seeking a highly skilled Clinical Study Manager to join our team at Parexel. The successful candidate will be responsible for managing and conducting start-up activities in compliance with client procedures, documents, local and international guidelines such as ICH-GCP and relevant regulations. Key responsibilities include preparing,...

Job SummaryWe are seeking a highly motivated and experienced Global Clinical Study Manager to join our team. As a key member of our medical team, you will be responsible for managing clinical studies and ensuring their successful execution.Key responsibilities include:Developing and implementing study plansCoordinating with internal stakeholders and...

Unlock Your Potential in Clinical OperationsParexel is seeking a dedicated Clinical Operations Leader to join our team in France. As a key member of our operations team, you will be responsible for supporting studies within your country or region, ensuring timely preparation of country financial Study Management Agreements and maintaining accurate study...

About the RoleParexel is seeking a Clinical Operations Leader to join our team in France. As a Local Study Associate Director, you will be responsible for supporting studies within your country or region.Key ResponsibilitiesManage local clinical trials, ensuring compliance with client procedural documents, international guidelines, and local regulations.Lead...

About the RolePfizer is seeking a highly skilled Country Study Operations Manager to join our team. As a key member of our medical team, you will be responsible for managing clinical studies and ensuring their successful execution.Key responsibilities include:Managing study timelines and budgetsCoordinating with internal stakeholders and vendorsEnsuring...

About the RoleParexel is seeking a highly skilled Clinical Operations Leader to join our team in France. As a key member of our clinical operations team, you will be responsible for supporting studies within your country or region.Key ResponsibilitiesManage and deliver committed components of clinical studies according to agreed resources, budget, and...

About the RoleWe are seeking a highly skilled and experienced Country Study Operations Manager to join our team at Pfizer. As a key member of our medical team, you will be responsible for managing clinical studies and ensuring their successful execution within time, budget, and scope.As a Country Study Operations Manager, you will provide guidance to...

Role OverviewWe are looking for a highly skilled and experienced Sr. Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements and study protocols.Key ResponsibilitiesProvide functional...

About this roleParexel is seeking a skilled Clinical Operations Leader to join our team in France. As a Local Study Associate Director, you will be responsible for supporting studies within your country or region, adhering to our mantra of 'manageable sites, manageable protocols.'Key responsibilitiesDeliver committed components of clinical studies according...

Job DescriptionPfizer is seeking a Global Study Operations Specialist to join our medical team. As a key member of our team, you will be responsible for managing clinical studies and leveraging your project management skills to plan, direct, and communicate timelines.You will partner with Global Study Managers, sCOM, Study Start Up Project Managers, Site...

Job DescriptionPfizer is seeking a highly skilled Regional Study Operations Lead to join our team. As a key member of our medical team, you will be responsible for managing clinical studies and ensuring their successful execution.Key responsibilities include:Developing and implementing study plansCoordinating with internal stakeholders and vendorsEnsuring...

Clinical Research Role at ExcelyaWe are seeking a Clinical Scientist to join our team at Excelya, a people-centered Contract Research Organization (CRO). In this role, you will support and represent the Study Medical Manager in all oncology study-related activities from set up to closure.Key Responsibilities:Contribute to the elaboration of trial documents,...

The Study Start-Up Manager is responsible for managing and conducting start-up activities in compliance with Client procedures, documents, and guidelines. Key responsibilities include providing regular information to Line Managers on study and planned study milestones, as well as supporting Study Management and Monitoring in different initiatives.Additional...

Study Start-Up Manager Job DescriptionThe Study Start-Up Manager is a critical role in ensuring the successful initiation and execution of clinical studies. As a key member of the study team, you will be responsible for managing and conducting start-up activities in compliance with client procedures, documents, and international guidelines such as ICH-GCP...

Job SummaryPfizer is seeking a Study Management Coordinator to join our medical team. As a key member of our team, you will be responsible for managing clinical studies and leveraging your project management skills to plan, direct, and communicate timelines.You will partner with Global Study Managers, sCOM, Study Start Up Project Managers, Site Intelligence...

About the RoleWe are seeking a highly experienced Senior Clinical Research Associate to join our global clinical trials team at Allucent. As a key member of our team, you will be responsible for monitoring and managing clinical studies to ensure compliance with regulatory requirements and Good Clinical Practice.Key ResponsibilitiesIndependently monitor and...

At Allucent, we are dedicated to supporting the success of small to medium-sized biopharmaceutical companies in navigating the complex landscape of clinical trials.We are seeking a highly experienced Senior Clinical Research Associate (CRA) to join our team. As a Senior CRA at Allucent, you will be responsible for independently monitoring and controlling...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies navigate the complex world of clinical trials to bring life-changing therapies to patients in need. We are seeking a Senior Clinical Research Associate to join our team, responsible for independently controlling and monitoring investigational sites, detecting issues, and...