Clinical Study Manager II

About the RoleWe are seeking a highly skilled Clinical Study Manager II to join our team at ICON. As a key member of our organization, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesLead the planning,...

Job SummaryWe are seeking a highly skilled Clinical Trial Manager II to join our team at Johnson & Johnson Sa De Cv. As a key member of our clinical operations team, you will be responsible for the local management of clinical trials in a country or countries.Key ResponsibilitiesCollaborate with Functional Manager and Clinical Research Manager to assess...

Job SummaryThe Clinical Study Manager will be responsible for managing, implementing, and monitoring clinical studies in a team setting according to ICON SOPs, SSPs, and all applicable rules and regulations.Key ResponsibilitiesIdentify, train, and initiate study sites, and close out study sites as needed.Conduct remote site monitoring visits and/or targeted...

About the RoleWe are seeking a highly skilled and experienced Clinical Study Manager to join our team at 520 Icr Mexico - Mex. As a Clinical Study Manager, you will be responsible for managing, implementing, and monitoring clinical studies, with support, in a team setting within a global organization.Key ResponsibilitiesComplete essential document collection...

Site Management AssociateAt ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical development. As a Site Management Associate, you'll play a critical role in managing, implementing, and monitoring clinical studies within a global organization.Key Responsibilities:Complete essential document...

Site Management AssociateAt ICON, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical development. As a Site Management Associate, you'll play a critical role in managing, implementing, and monitoring clinical studies within a global organization.Key Responsibilities:Complete essential document collection...

Job SummaryWe are seeking a highly skilled Clinical Project Manager to join our team at Novartis. As a Clinical Project Manager, you will be responsible for the day-to-day planning, execution, and reporting of assigned Global Drug Development studies in compliance with Novartis processes and regulatory requirements.Key ResponsibilitiesDevelop and execute...

Job SummaryThe Clinical Trial Manager II is responsible for the local management of clinical trials in a country or countries. This role is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocols from start-up through to database lock and closeout activities.Key ResponsibilitiesCollaborate with...

Job Title: Clinical Research CoordinatorLocation: Houston, TexasCompany: Clinical Trial NetworkPosition Type: Full-timeVisa: TN offeredWe are seeking a highly organized and experienced Clinical Research Coordinator to play a critical role in the planning, implementation, and coordination of clinical research studies conducted within Clinical Trial...

About the RoleWe are seeking a highly skilled Clinical Specialist II to join our team in Monterrey, Mexico. As a Clinical Specialist II, you will play a critical role in assisting the Clinical department and hospital research team during the conduct of studies, as well as after procedures, in all study-required data collection.Key ResponsibilitiesAssist in...

Job Title: Senior Clinical Research Associate IIAt Psi Cro, we are committed to delivering high-quality clinical research services that make a real difference in people's lives. As a Senior Clinical Research Associate II, you will play a key role in facilitating regional projects, supervising study activities, and ensuring compliance with regulatory...

**Job Summary:**The Clinical Study Coordinator will play a critical role in the conduct of clinical research studies at Avantgarde Human Capital Consultants. This position will support the site's Principal Investigator in the development, monitoring, implementation, and closeout of assigned protocols.**Key Responsibilities:**• Develop and maintain a...

About the RoleAs a Site Management Associate at ICON, you will play a crucial role in managing, implementing, and monitoring clinical studies. You will be responsible for ensuring the smooth execution of studies, from site activation to close-out. Your primary focus will be on managing electronic Trial Master Files, conducting remote site monitoring visits,...

Study Start Up Associate IIAt Icon, we are seeking a highly skilled Study Start Up Associate II to join our team. As a key member of our study start up team, you will be responsible for collecting, preparing, reviewing, approving, processing, and tracking regulatory and site-level critical documents required for study site activation.Key...

{"title": "Study Start Up Associate II", "content": "About the RoleAs a Study Start Up Associate II, you will play a critical role in ensuring the successful start-up of clinical trials at our research sites. Your expertise in contract negotiation and budget analysis will be essential in reviewing and negotiating clinical site investigator contracts and...

About Psi Cro AgPsi Cro Ag is a leading Contract Research Organization with a rich history of delivering high-quality services across various therapeutic indications. Our organization prides itself on striking a perfect balance between stability and innovation, providing a dynamic work environment for our employees and clients alike.Job SummaryWe are seeking...

About the RoleAs a Clinical Trial Manager II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesCollaborate with cross-functional teams to develop and implement comprehensive clinical trial...

{"title": "Senior Study Operations Manager", "content": "Job SummaryAbbVie is seeking a Senior Study Operations Manager to join our Clinical Study Leadership team. As a people leader, you will be responsible for managing a regional team of Study Management Associates, providing guidance and support to ensure best-in-class study execution.Key...

Job SummaryAs a Clinical Trials Manager I Client Based Mexico, you will be responsible for overseeing site management, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.Key ResponsibilitiesResponsible for site management oversight, clinical monitoring, and central...

Job SummaryWe are seeking a highly skilled and experienced Clinical Trials Manager to join our team at Amgen. As a key member of our clinical operations team, you will be responsible for leading and managing the conduct of clinical trials from study start-up to close out at a country level.Key ResponsibilitiesPartner with global and local country teams to...