Clinical Trials Manager

Clinical Trial ManagerWe are seeking a highly skilled Clinical Trial Manager to join our team at ICON plc. As a key member of our research department, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials.Key Responsibilities:Plan and manage all aspects of clinical trials, ensuring adherence to...

Job SummaryWe are seeking a highly skilled Clinical Trials Specialist to join our team at Syneos Health. As a key member of our clinical development team, you will be responsible for ensuring the smooth start-up of investigative sites in all phases of clinical trials.Key Responsibilities:Deliver high-quality site start-up activities within agreed timelines...

About the Role:We are seeking a skilled Clinical Payment Specialist to join our team at Worldwide Clinical Trials. As a Clinical Payment Specialist, you will be responsible for the end-to-end management of global Investigator payments for assigned studies.Key Responsibilities:Manage the set-up, deployment, and close-out of study payments solutionsPerform...

About This OpportunityWe are seeking a skilled Clinical Assessment Technologist to join our team at Worldwide Clinical Trials. This role will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.Key ResponsibilitiesAssist in reviewing eCOA/ePRO specifications and engaging in User Acceptance...

Job Title: Clinical Trials Project ManagerJob Summary:We are seeking a highly skilled Clinical Trials Project Manager to join our team at ICON Plc. As a Clinical Trials Project Manager, you will be responsible for managing projects in a timely manner, adhering to ICON's SOPs, ICH, GCP, and relevant regulations. You will also be responsible for delivering...

Job Title: Clinical Research ManagerFortrea is seeking a highly skilled Clinical Research Manager to join our team. As a Clinical Research Manager, you will be responsible for managing clinical trials from start to finish, ensuring that all studies are conducted in accordance with regulatory requirements and company standards.Key Responsibilities:Manage...

About the RoleThe Team Lead, TMF Operations at Worldwide Clinical Trials is responsible for ensuring Trial Master Files are inspection-ready and compliant with relevant Standard Operating Procedures, ALCOA principles, country regulations, and industry best practices.Key ResponsibilitiesDrive the delivery of Project Team objectives in managing essential...

Job SummaryWe are seeking a highly skilled Clinical Operations Manager to contribute to the success of our global clinical trials. As a key member of the Clinical Trial Team, you will be responsible for delivering study outcomes within schedule, budget, quality, and performance standards.About the RoleThe Clinical Operations Manager will be responsible...

At ICON plc, we're seeking a skilled Clinical Trials Specialist to join our dynamic team. As a key member of our team, 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 Responsibilities:Review and analyze contracts,...

**Clinical Trials Associate - ICON Plc**ICON Plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment driving innovation and excellence.The key responsibilities of this role include:Providing administrative support to the Project Manager(s), Clinical Trial Manager(s), and/or...

Job Title: Clinical Trials Document SpecialistFortrea is seeking a highly organized and detail-oriented Clinical Trials Document Specialist to join our team. As a key member of our clinical development team, you will be responsible for maintaining the integrity and accuracy of clinical trial documents.Key Responsibilities:Organize and maintain clinical trial...

Job SummaryWe are seeking a highly skilled Clinical Development Manager to join our team at Novartis. As a key member of our Clinical Operations team, you will be responsible for overseeing and coordinating program and study level feasibility assessments in the country or extended country group.About the RoleThis is a critical role that requires strong...

About Thermo Fisher Scientific Inc.We are a world-class company at the forefront of enabling customers to make the world healthier, cleaner, and safer.As a global leader in serving science, we are committed to providing exceptional solutions that accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in...

Job SummaryThermo Fisher Scientific is seeking a highly motivated and detail-oriented Clinical Trials Coordinator (Level II) to join our team. In this role, you will provide support for clinical trials, medical research, and health care projects.Work Schedule: Flexible schedule to meet the needs of the team and projects.Environmental Conditions: Office...

Job Title: Associate II, TMF OperationsWe are seeking a highly organized and detail-oriented Associate II, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating...

Senior Centralized Clinical Trial ManagerAt ICON, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a Senior Centralized Clinical Trial Manager to join our diverse and dynamic team.Key Responsibilities:Develop and implement comprehensive operational strategies to streamline centralized clinical trial...

Job Title: Senior Associate I, TMF OperationsWe are seeking a highly skilled Senior Associate I, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating Procedures, ALCOA...

As a Clinical Trials Project Coordinator at Novo Nordisk, you will be responsible for overseeing the lifecycle management of clinical and real-world evidence Investigator Sponsored Studies (ISS), ensuring seamless coordination from project initiation to completion.**Key Responsibilities:**Manage Research Grants Committee ISS review meetings by sending...

About the RoleWe are seeking a highly skilled Senior Clinical Trial Manager to join our team at Novartis. As a key member of our clinical operations team, you will be responsible for the timely and efficient execution of clinical trials, ensuring compliance with quality standards and regulatory requirements.Key ResponsibilitiesLead the study start-up...

About the RoleWe are seeking a highly skilled and experienced SSU Manager to join our team at Novartis. As a key member of our clinical operations team, you will be responsible for contributing to the successful delivery of global clinical trials.Key Responsibilities:Contribute to the planning, execution, and monitoring of clinical trials to ensure timely...